@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:NP150316.RAuExmVDDhTtawu2FpRHWQB16FsDXlLdCZL-Aku9-1UYk130_head { this: np:hasAssertion dgn-np:NP150316.RAuExmVDDhTtawu2FpRHWQB16FsDXlLdCZL-Aku9-1UYk130_assertion; np:hasProvenance dgn-np:NP150316.RAuExmVDDhTtawu2FpRHWQB16FsDXlLdCZL-Aku9-1UYk130_provenance; np:hasPublicationInfo dgn-np:NP150316.RAuExmVDDhTtawu2FpRHWQB16FsDXlLdCZL-Aku9-1UYk130_publicationInfo; a np:Nanopublication . dgn-np:NP150316.RAuExmVDDhTtawu2FpRHWQB16FsDXlLdCZL-Aku9-1UYk130_assertion a np:Assertion . dgn-np:NP150316.RAuExmVDDhTtawu2FpRHWQB16FsDXlLdCZL-Aku9-1UYk130_provenance a np:Provenance . dgn-np:NP150316.RAuExmVDDhTtawu2FpRHWQB16FsDXlLdCZL-Aku9-1UYk130_publicationInfo a np:PublicationInfo . } dgn-np:NP150316.RAuExmVDDhTtawu2FpRHWQB16FsDXlLdCZL-Aku9-1UYk130_assertion { miriam-gene:6256 a ncit:C16612 . lld:C1527249 a ncit:C7057 . dgn-gda:DGN74afbd9179c20ec6c94d991707c36209 sio:SIO_000628 miriam-gene:6256, lld:C1527249; a sio:SIO_001122 . } dgn-np:NP150316.RAuExmVDDhTtawu2FpRHWQB16FsDXlLdCZL-Aku9-1UYk130_provenance { dgn-np:NP150316.RAuExmVDDhTtawu2FpRHWQB16FsDXlLdCZL-Aku9-1UYk130_assertion dcterms:description "[However, for RXRA SNP rs7861779, a high-interest SNP selected for study a priori, there was a statistically significantly increased risk for proximal colorectal cancer among those with at least one A allele odds ratio (OR) = 1.42; 95% confidence interval (CI) = 1.03-1.97.]. 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:20558521; 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:NP150316.RAuExmVDDhTtawu2FpRHWQB16FsDXlLdCZL-Aku9-1UYk130_publicationInfo { this: dcterms:created "2015-08-25T14:39:05+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" . }