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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking NDUFB11 and linear skin defects with multiple congenital anomalies 1 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
  • 5 RGD objects have been annotated to linear skin defects with multiple congenital anomalies 1  (DOID:0111808)
  • 4 papers in RGD have been used to annotate NDUFB11
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking NDUFB11 and linear skin defects with multiple congenital anomalies 1 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:10044820 (Homo sapiens)
  • 5 RGD objects have been annotated to linear skin defects with multiple congenital anomalies 1  (DOID:0111808)
  • 4 papers in RGD have been used to annotate NDUFB11
  • Curation Notes: ClinVar Annotator: match by term: Linear skin defects with multiple congenital anomalies 1
  • Original References(s): PMID:25741868 PMID:25772934


    • An association has been curated linking NDUFB11 and linear skin defects with multiple congenital anomalies 1 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:14702524 (Homo sapiens)
  • 5 RGD objects have been annotated to linear skin defects with multiple congenital anomalies 1  (DOID:0111808)
  • 4 papers in RGD have been used to annotate NDUFB11
  • Curation Notes: ClinVar Annotator: match by term: Linear skin defects with multiple congenital anomalies 1
  • Original References(s): PMID:25741868


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