@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:NP439321.RAu-ykrXgUVMghyhGdYXJGDG__i19Fn0VzsIyYHhUsnEg130_head { this: np:hasAssertion dgn-np:NP439321.RAu-ykrXgUVMghyhGdYXJGDG__i19Fn0VzsIyYHhUsnEg130_assertion; np:hasProvenance dgn-np:NP439321.RAu-ykrXgUVMghyhGdYXJGDG__i19Fn0VzsIyYHhUsnEg130_provenance; np:hasPublicationInfo dgn-np:NP439321.RAu-ykrXgUVMghyhGdYXJGDG__i19Fn0VzsIyYHhUsnEg130_publicationInfo; a np:Nanopublication . dgn-np:NP439321.RAu-ykrXgUVMghyhGdYXJGDG__i19Fn0VzsIyYHhUsnEg130_assertion a np:Assertion . dgn-np:NP439321.RAu-ykrXgUVMghyhGdYXJGDG__i19Fn0VzsIyYHhUsnEg130_provenance a np:Provenance . dgn-np:NP439321.RAu-ykrXgUVMghyhGdYXJGDG__i19Fn0VzsIyYHhUsnEg130_publicationInfo a np:PublicationInfo . } dgn-np:NP439321.RAu-ykrXgUVMghyhGdYXJGDG__i19Fn0VzsIyYHhUsnEg130_assertion { miriam-gene:2950 a ncit:C16612 . lld:C0017638 a ncit:C7057 . dgn-gda:DGN678c8758f29fd153e95018391d77a007 sio:SIO_000628 miriam-gene:2950, lld:C0017638; a sio:SIO_001122 . } dgn-np:NP439321.RAu-ykrXgUVMghyhGdYXJGDG__i19Fn0VzsIyYHhUsnEg130_provenance { dgn-np:NP439321.RAu-ykrXgUVMghyhGdYXJGDG__i19Fn0VzsIyYHhUsnEg130_assertion dcterms:description "[The quantitative synthesis showed no significant evidence to indicate an association exists between the presence of a GSTM1, GSTT1 or GSTP1 Ile105Val haplotype polymorphism and the risk of adult gliomas (OR, 1.008, 1.246, 1.061 respectively; 95% CI, 0.901-1.129, 0.963-1.611, 0.653-1.724 respectively).]. 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:22502660; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP439321.RAu-ykrXgUVMghyhGdYXJGDG__i19Fn0VzsIyYHhUsnEg130_publicationInfo { this: dcterms:created "2015-08-25T14:41:56+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" . }