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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Apoe and Coronary Disease in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Viitanen L, etal., J Mol Med. 2001 Dec;79(12):732-7. Epub 2001 Jul 25.
  • The annotation has been inferred from sequence orthology with APOE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Viitanen L, etal., J Mol Med. 2001 Dec;79(12):732-7. Epub 2001 Jul 25.
  • 621 RGD objects have been annotated to Coronary Disease  (DOID:9000528)
  • 155 papers in RGD have been used to annotate Apoe
  • Curation Notes: DNA:polymorphisms, haplotype:promoter, cds:g.-219G>T, p.C112R, p.R158C (human)


    • An association has been curated linking Apoe and Coronary Disease 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 APOE (Homo sapiens) [(EXP) inferred from experiment]
  • 621 RGD objects have been annotated to Coronary Disease  (DOID:9000528)
  • 155 papers in RGD have been used to annotate Apoe
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:10736278


    • An association has been curated linking Apoe and Coronary Disease in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Automated assignment of GO, PW and RDO ISO annotations across species
  • The annotation has been inferred from sequence orthology with APOE (Homo sapiens)
  • 621 RGD objects have been annotated to Coronary Disease  (DOID:9000528)
  • 155 papers in RGD have been used to annotate Apoe
  • Qualifier: onset
  • Curation Notes: DNA:polymorphisms, haplotype:promoter, cds:g.-219G>T, p.C112R, p.R158C (human)
  • Original References(s): PMID:11862316 REF_RGD_ID:1578479


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