@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:NP1096242.RAv4FtbWur70ws8Pc-XaVDn8WgaO-DdLLI1iuJV8oGVkM130_head { this: np:hasAssertion dgn-np:NP1096242.RAv4FtbWur70ws8Pc-XaVDn8WgaO-DdLLI1iuJV8oGVkM130_assertion; np:hasProvenance dgn-np:NP1096242.RAv4FtbWur70ws8Pc-XaVDn8WgaO-DdLLI1iuJV8oGVkM130_provenance; np:hasPublicationInfo dgn-np:NP1096242.RAv4FtbWur70ws8Pc-XaVDn8WgaO-DdLLI1iuJV8oGVkM130_publicationInfo; a np:Nanopublication . dgn-np:NP1096242.RAv4FtbWur70ws8Pc-XaVDn8WgaO-DdLLI1iuJV8oGVkM130_assertion a np:Assertion . dgn-np:NP1096242.RAv4FtbWur70ws8Pc-XaVDn8WgaO-DdLLI1iuJV8oGVkM130_provenance a np:Provenance . dgn-np:NP1096242.RAv4FtbWur70ws8Pc-XaVDn8WgaO-DdLLI1iuJV8oGVkM130_publicationInfo a np:PublicationInfo . } dgn-np:NP1096242.RAv4FtbWur70ws8Pc-XaVDn8WgaO-DdLLI1iuJV8oGVkM130_assertion { miriam-gene:1312 a ncit:C16612 . lld:C0007102 a ncit:C7057 . dgn-gda:DGN9b8b92c4b3c7f0bcc8a45688bbb4e7d9 sio:SIO_000628 miriam-gene:1312, lld:C0007102; a sio:SIO_001121 . } dgn-np:NP1096242.RAv4FtbWur70ws8Pc-XaVDn8WgaO-DdLLI1iuJV8oGVkM130_provenance { dgn-np:NP1096242.RAv4FtbWur70ws8Pc-XaVDn8WgaO-DdLLI1iuJV8oGVkM130_assertion dcterms:description "[We identified 10 single nucleotide polymorphisms that tagged variation across two isoforms of COMT in 2,458 women with CRC from the Nurses' Health Study, Postmenopausal Hormones Supplementary Study to the Colon Cancer Family Registry, VITamins And Lifestyle Study, and Women's Health Initiative.]. 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:23880798; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1096242.RAv4FtbWur70ws8Pc-XaVDn8WgaO-DdLLI1iuJV8oGVkM130_publicationInfo { this: dcterms:created "2016-05-13T12:50:03+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }