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GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking EBP and MEND syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10404665 (Homo sapiens)
  • 1 RGD objects have been annotated to MEND syndrome  (DOID:0111865)
  • 9 papers in RGD have been used to annotate EBP
  • Curation Notes: ClinVar Annotator: match by term: MEND syndrome
  • Original References(s): PMID:24459067


    • An association has been curated linking EBP and MEND syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9682437 (Homo sapiens)
  • 1 RGD objects have been annotated to MEND syndrome  (DOID:0111865)
  • 9 papers in RGD have been used to annotate EBP
  • Curation Notes: ClinVar Annotator: match by term: MEND syndrome
  • Original References(s): PMID:18414213 PMID:20949533


    • An association has been curated linking EBP and MEND syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10406257 (Homo sapiens)
  • 1 RGD objects have been annotated to MEND syndrome  (DOID:0111865)
  • 9 papers in RGD have been used to annotate EBP
  • Curation Notes: ClinVar Annotator: match by term: MEND syndrome
  • Original References(s): PMID:23307567 PMID:24700572


    • An association has been curated linking EBP and MEND syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to MEND syndrome  (DOID:0111865)
  • 9 papers in RGD have been used to annotate EBP


    • An association has been curated linking EBP and MEND syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8562522 (Homo sapiens)
  • 1 RGD objects have been annotated to MEND syndrome  (DOID:0111865)
  • 9 papers in RGD have been used to annotate EBP
  • Curation Notes: ClinVar Annotator: match by term: MEND syndrome
  • Original References(s): PMID:11038443 PMID:12503101 PMID:12966533


    • An association has been curated linking EBP and MEND syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9682438 (Homo sapiens)
  • 1 RGD objects have been annotated to MEND syndrome  (DOID:0111865)
  • 9 papers in RGD have been used to annotate EBP
  • Curation Notes: ClinVar Annotator: match by term: MEND syndrome
  • Original References(s): PMID:18414213 PMID:25741868 PMID:28492532


    • An association has been curated linking EBP and MEND syndrome in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to MEND syndrome  (DOID:0111865)
  • 9 papers in RGD have been used to annotate EBP
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking EBP and MEND syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10449876 (Homo sapiens)
  • 1 RGD objects have been annotated to MEND syndrome  (DOID:0111865)
  • 9 papers in RGD have been used to annotate EBP
  • Curation Notes: ClinVar Annotator: match by term: MALE EBP DISORDER WITH NEUROLOGIC DEFECTS
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking EBP and MEND syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11559947|RGD:151728455|RGD:401948316 (Homo sapiens) & RGD:11559947|RGD:151728455|RGD:401948316 (Homo sapiens) & RGD:11559947|RGD:151728455|RGD:401948316 (Homo sapiens)
  • 1 RGD objects have been annotated to MEND syndrome  (DOID:0111865)
  • 9 papers in RGD have been used to annotate EBP
  • Curation Notes: ClinVar Annotator: match by term: MEND syndrome
  • Original References(s): PMID:25741868


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