@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP124781.RAAsG1FEjv3guiFnoYT94kFkxg1ufqlwl1Vf3tjYPXcl4130_head { this: np:hasAssertion dgn-np:NP124781.RAAsG1FEjv3guiFnoYT94kFkxg1ufqlwl1Vf3tjYPXcl4130_assertion; np:hasProvenance dgn-np:NP124781.RAAsG1FEjv3guiFnoYT94kFkxg1ufqlwl1Vf3tjYPXcl4130_provenance; np:hasPublicationInfo dgn-np:NP124781.RAAsG1FEjv3guiFnoYT94kFkxg1ufqlwl1Vf3tjYPXcl4130_publicationInfo; a np:Nanopublication . dgn-np:NP124781.RAAsG1FEjv3guiFnoYT94kFkxg1ufqlwl1Vf3tjYPXcl4130_assertion a np:Assertion . dgn-np:NP124781.RAAsG1FEjv3guiFnoYT94kFkxg1ufqlwl1Vf3tjYPXcl4130_provenance a np:Provenance . dgn-np:NP124781.RAAsG1FEjv3guiFnoYT94kFkxg1ufqlwl1Vf3tjYPXcl4130_publicationInfo a np:PublicationInfo . } dgn-np:NP124781.RAAsG1FEjv3guiFnoYT94kFkxg1ufqlwl1Vf3tjYPXcl4130_assertion { miriam-gene:10599 a ncit:C16612 . lld:C1956346 a ncit:C7057 . dgn-gda:DGN85de2b3d55e486f2dab510404ec8d3b2 sio:SIO_000628 miriam-gene:10599, lld:C1956346; a sio:SIO_001122 . } dgn-np:NP124781.RAAsG1FEjv3guiFnoYT94kFkxg1ufqlwl1Vf3tjYPXcl4130_provenance { dgn-np:NP124781.RAAsG1FEjv3guiFnoYT94kFkxg1ufqlwl1Vf3tjYPXcl4130_assertion dcterms: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."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:19238116; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP124781.RAAsG1FEjv3guiFnoYT94kFkxg1ufqlwl1Vf3tjYPXcl4130_publicationInfo { this: dcterms:created "2015-08-25T14:38:50+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }