@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:NP140475.RATntJ65hnaTKqms_INzEe7Yw49H3lrpBft6-_Hlpew1A130_head { this: np:hasAssertion dgn-np:NP140475.RATntJ65hnaTKqms_INzEe7Yw49H3lrpBft6-_Hlpew1A130_assertion; np:hasProvenance dgn-np:NP140475.RATntJ65hnaTKqms_INzEe7Yw49H3lrpBft6-_Hlpew1A130_provenance; np:hasPublicationInfo dgn-np:NP140475.RATntJ65hnaTKqms_INzEe7Yw49H3lrpBft6-_Hlpew1A130_publicationInfo; a np:Nanopublication . dgn-np:NP140475.RATntJ65hnaTKqms_INzEe7Yw49H3lrpBft6-_Hlpew1A130_assertion a np:Assertion . dgn-np:NP140475.RATntJ65hnaTKqms_INzEe7Yw49H3lrpBft6-_Hlpew1A130_provenance a np:Provenance . dgn-np:NP140475.RATntJ65hnaTKqms_INzEe7Yw49H3lrpBft6-_Hlpew1A130_publicationInfo a np:PublicationInfo . } dgn-np:NP140475.RATntJ65hnaTKqms_INzEe7Yw49H3lrpBft6-_Hlpew1A130_assertion { miriam-gene:2065 a ncit:C16612 . lld:C0011860 a ncit:C7057 . dgn-gda:DGNf57e757f10c2877563ee79b86b3d8ed2 sio:SIO_000628 miriam-gene:2065, lld:C0011860; a sio:SIO_001122 . } dgn-np:NP140475.RATntJ65hnaTKqms_INzEe7Yw49H3lrpBft6-_Hlpew1A130_provenance { dgn-np:NP140475.RATntJ65hnaTKqms_INzEe7Yw49H3lrpBft6-_Hlpew1A130_assertion dcterms:description "[These results suggest that individuals with increased genetic susceptibility to T2D have decreased risk for PCa. This association is consistent with the observation that individuals with T2D are at decreased risk for PCa; however, data on T2D status was n]. 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:20203524; 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:NP140475.RATntJ65hnaTKqms_INzEe7Yw49H3lrpBft6-_Hlpew1A130_publicationInfo { this: dcterms:created "2015-08-25T14:38:59+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" . }