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- source_evidence_literature type ECO_0000212 NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_provenance.
- NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_assertion description "[Four significant associations with CAD were detected after controlling age and the false discovery rate at 15%: the recessive effect of SNP rs887829 (UGT1A1 G-364A) age-adjusted odds ratio (OR): 0.24; 95% confidence interval (CI): 0.10-0.60; P=0.0014 and dominant effect of rs4149013 (SLCO1B1 A-12099G) (age-adjusted OR: 0.70; 95% CI: 0.55-0.91; P=0.0069) on male CAD, and the additive effects of rs2877262 (BLVRA G+1238/in6C) (age-adjusted OR: 0.73; 95% CI: 0.59-0.89; P=0.0021) and rs2690381 (BLVRA G+2613/in6A) (age-adjusted OR: 0.70; 95% CI: 0.56-0.86; P=0.0008) on female CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_provenance.
- NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_assertion evidence source_evidence_literature NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_provenance.
- NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_assertion SIO_000772 19238116 NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_provenance.
- NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_assertion wasDerivedFrom gad-20150221 NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_provenance.
- NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_assertion wasGeneratedBy ECO_0000203 NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP125479.RAObGtK8ARun0k8nfeqjDrUte3YB-fhveLdWdUDYwemCc130_provenance.