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GENE - TERM ANNOTATION REPORT

69 Annotations Found.

An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Miceli-Richard C, etal., Nat Genet. 2001 Sep;29(1):19-20.
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 additional annotations were made from Miceli-Richard C, etal., Nat Genet. 2001 Sep;29(1):19-20.
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Qualifier: susceptibility
  • Curation Notes: DNA:snps:cds:p.R334Q, p.R334W, p.L469F (human)


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from van Duist MM, etal., Eur J Hum Genet. 2005 Jun;13(6):742-7.
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from van Duist MM, etal., Eur J Hum Genet. 2005 Jun;13(6):742-7.
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Qualifier: susceptibility
  • Curation Notes: DNA:snp:cds:p.E383K (human)


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Rose CD, etal., Arthritis Rheum. 2009 Jun;60(6):1797-803. doi: 10.1002/art.24533.
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Rose CD, etal., Arthritis Rheum. 2009 Jun;60(6):1797-803. doi: 10.1002/art.24533.
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Qualifier: susceptibility
  • Curation Notes: DNA:snps:cds:p.R587C, p.C495Y, p.W490L (human)


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Okafuji I, etal., Arthritis Rheum. 2009 Jan;60(1):242-50. doi: 10.1002/art.24134.
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 additional annotations were made from Okafuji I, etal., Arthritis Rheum. 2009 Jan;60(1):242-50. doi: 10.1002/art.24134.
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Qualifier: susceptibility
  • Curation Notes: DNA:snp:cds:p.E383G (human)


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by OMIM:186580
  • Original References(s): PMID:11528384


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:28492532 PMID:29697845


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:11528384 PMID:15086578 PMID:15459013 PMID:19467619


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Sarcoidosis, early-onset
  • Original References(s): PMID:15459013


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by OMIM:186580


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755 PMID:12626759 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11528384 PMID:12626759 PMID:14522785 PMID:15044951 PMID:15459013 PMID:15554080 PMID:17157607 PMID:17207093 PMID:17393391 PMID:20084402 PMID:20199415 PMID:22509093 PMID:24713464 PMID:25093298 PMID:25416713 PMID:25429073 PMID:26606664 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:16278823 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:17968944 PMID:19116920 PMID:19479837 PMID:20039400 PMID:25093298 PMID:28639104


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11528384 PMID:14522785 PMID:15044951 PMID:15086578 PMID:15459013 PMID:17157607 PMID:17207093 PMID:18955195 PMID:20199415 PMID:22509093 PMID:24713464 PMID:25416713 PMID:28492532 PMID:9124059


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:24033266


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:18507017 PMID:20230816 PMID:24033266


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:28492532 PMID:30166421


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:22470564 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:28492532 PMID:29503906


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:24595243 PMID:28492532 PMID:29248579


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11087742 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:16278823 PMID:16804397 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:27306066 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15024686 PMID:21983784 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15812565 PMID:18718560 PMID:19479836 PMID:20565245 PMID:25093298 PMID:25136265 PMID:25829188 PMID:27339507 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:11385577 PMID:11425413 PMID:11910337 PMID:12019468 PMID:12512038 PMID:15024686 PMID:15190267 PMID:15198989 PMID:15571588 PMID:18240302 PMID:18489434 PMID:19713276 PMID:21335489 PMID:21548950 PMID:22684479 PMID:26500656 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755 PMID:16278823 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:12115249 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755 PMID:15459013 PMID:7825454


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15998797 PMID:16278823 PMID:16804397 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:11875755 PMID:12115249 PMID:12626759 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:24876985 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15024686 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:11875755 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:11385577 PMID:12019468 PMID:12512038 PMID:12557156 PMID:15024686 PMID:15190267 PMID:15198989 PMID:15571588 PMID:18489434 PMID:19713276 PMID:21548950 PMID:21830272 PMID:26070941 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755 PMID:15044951 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:11875755 PMID:12626759 PMID:15459013 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755 PMID:12626759 PMID:16485124 PMID:26500656 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:11875755 PMID:12626759 PMID:16485124 PMID:21983784 PMID:25741868 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:11875755 PMID:12626759 PMID:14508222 PMID:15044951 PMID:15770725 PMID:25741868 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:11875755 PMID:15024686 PMID:15712650 PMID:22319155 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:23334666 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:16485124 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15459013 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:11875755 PMID:12626759 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:11875755 PMID:12115249 PMID:15044951 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:17941079 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15044951 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:12630966 PMID:22926499


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755 PMID:12626759 PMID:20032092 PMID:26316104 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:16485124


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15712650 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:15024686 PMID:26500656 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:11875755 PMID:12626759 PMID:15024686 PMID:18056399 PMID:24960071 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:25741868 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:12577202 PMID:14765395 PMID:15024686 PMID:19467619 PMID:21914217 PMID:23102769 PMID:25741868 PMID:26070941 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11385576 PMID:25741868


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755 PMID:15044951 PMID:18419343 PMID:24391456 PMID:24583628 PMID:28492532 PMID:28814775


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Blau syndrome
  • Original References(s): PMID:11875755 PMID:12626759 PMID:15024686 PMID:15320482 PMID:15770725 PMID:16278823 PMID:21983784 PMID:22942351 PMID:24803813 PMID:26164256 PMID:28492532


  • An association has been curated linking Nod2 and Blau syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NOD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Blau syndrome  (DOID:0050678)
  • 72 papers in RGD have been used to annotate Nod2
  • Curation Notes: ClinVar Annotator: match by term: Jabs syndrome
  • Original References(s): PMID:11385576 PMID:11875755 PMID:12019468 PMID:12512038 PMID:15024686 PMID:15198989 PMID:15571588 PMID:15770725 PMID:15967635 PMID:18240302 PMID:18489434 PMID:18541930 PMID:19713276 PMID:20959815 PMID:21274544 PMID:21548950 PMID:21830272 PMID:21914217 PMID:22684479 PMID:23102769 PMID:24033266 PMID:26070941 PMID:28492532


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