@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:NP50780.RAZYs1vg8J0mSWrrnJYk7VKkn6lMe2AHsPATNviH2Gy0g130_head { this: np:hasAssertion dgn-np:NP50780.RAZYs1vg8J0mSWrrnJYk7VKkn6lMe2AHsPATNviH2Gy0g130_assertion; np:hasProvenance dgn-np:NP50780.RAZYs1vg8J0mSWrrnJYk7VKkn6lMe2AHsPATNviH2Gy0g130_provenance; np:hasPublicationInfo dgn-np:NP50780.RAZYs1vg8J0mSWrrnJYk7VKkn6lMe2AHsPATNviH2Gy0g130_publicationInfo; a np:Nanopublication . dgn-np:NP50780.RAZYs1vg8J0mSWrrnJYk7VKkn6lMe2AHsPATNviH2Gy0g130_assertion a np:Assertion . dgn-np:NP50780.RAZYs1vg8J0mSWrrnJYk7VKkn6lMe2AHsPATNviH2Gy0g130_provenance a np:Provenance . dgn-np:NP50780.RAZYs1vg8J0mSWrrnJYk7VKkn6lMe2AHsPATNviH2Gy0g130_publicationInfo a np:PublicationInfo . } dgn-np:NP50780.RAZYs1vg8J0mSWrrnJYk7VKkn6lMe2AHsPATNviH2Gy0g130_assertion { miriam-gene:2947 a ncit:C16612 . lld:C0242379 a ncit:C7057 . dgn-gda:DGN005e7e1de201b47ed616122ad9eda65d sio:SIO_000628 miriam-gene:2947, lld:C0242379; a sio:SIO_001122 . } dgn-np:NP50780.RAZYs1vg8J0mSWrrnJYk7VKkn6lMe2AHsPATNviH2Gy0g130_provenance { dgn-np:NP50780.RAZYs1vg8J0mSWrrnJYk7VKkn6lMe2AHsPATNviH2Gy0g130_assertion dcterms:description "[While adjusted odds ratios (ORs) indicated no significantly increased risk for lung cancer overall due to any single GST genotype, the risk alleles for GSTM1, GSTM3 and GSTP1 conferring reduced enzyme activity were present at higher frequency in SCC than in AC patients.]. 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:11740339; 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:NP50780.RAZYs1vg8J0mSWrrnJYk7VKkn6lMe2AHsPATNviH2Gy0g130_publicationInfo { this: dcterms:created "2015-08-25T14:38:08+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" . }