@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:NP991078.RAALVWNgyZRI3Nrz2LSMZUAsqPlZnZqtOEjg6_loSGFPQ130_head { this: np:hasAssertion dgn-np:NP991078.RAALVWNgyZRI3Nrz2LSMZUAsqPlZnZqtOEjg6_loSGFPQ130_assertion; np:hasProvenance dgn-np:NP991078.RAALVWNgyZRI3Nrz2LSMZUAsqPlZnZqtOEjg6_loSGFPQ130_provenance; np:hasPublicationInfo dgn-np:NP991078.RAALVWNgyZRI3Nrz2LSMZUAsqPlZnZqtOEjg6_loSGFPQ130_publicationInfo; a np:Nanopublication . dgn-np:NP991078.RAALVWNgyZRI3Nrz2LSMZUAsqPlZnZqtOEjg6_loSGFPQ130_assertion a np:Assertion . dgn-np:NP991078.RAALVWNgyZRI3Nrz2LSMZUAsqPlZnZqtOEjg6_loSGFPQ130_provenance a np:Provenance . dgn-np:NP991078.RAALVWNgyZRI3Nrz2LSMZUAsqPlZnZqtOEjg6_loSGFPQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP991078.RAALVWNgyZRI3Nrz2LSMZUAsqPlZnZqtOEjg6_loSGFPQ130_assertion { miriam-gene:391109 a ncit:C16612 . lld:C0242379 a ncit:C7057 . dgn-gda:DGN0cb4fb7ef74a4b396d7eb05b1963f02c sio:SIO_000628 miriam-gene:391109, lld:C0242379; a sio:SIO_001121 . } dgn-np:NP991078.RAALVWNgyZRI3Nrz2LSMZUAsqPlZnZqtOEjg6_loSGFPQ130_provenance { dgn-np:NP991078.RAALVWNgyZRI3Nrz2LSMZUAsqPlZnZqtOEjg6_loSGFPQ130_assertion dcterms:description "[The combined 'at risk' genotypes of GSTM1 null and GSTT1 null in comparison with 'wild-type' genotypes seems to be associated with a greater risk of lung cancer, but the results are not significant (odds ratio (OR) 2.0, 95% confidence interval (CI) 0.68-5.96) and for squamous cell carcinoma (SqCC) it was 1.6-fold (OR 1.6, 95% CI 0.49-5.68).]. 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:18415801; 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:NP991078.RAALVWNgyZRI3Nrz2LSMZUAsqPlZnZqtOEjg6_loSGFPQ130_publicationInfo { this: dcterms:created "2015-08-25T14:47:48+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" . }