@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:NP1364241.RAZqaQ3QxVA_v6zdDuHIK30oed8tzsNF4QSuddsZfGSPA130_head { this: np:hasAssertion dgn-np:NP1364241.RAZqaQ3QxVA_v6zdDuHIK30oed8tzsNF4QSuddsZfGSPA130_assertion; np:hasProvenance dgn-np:NP1364241.RAZqaQ3QxVA_v6zdDuHIK30oed8tzsNF4QSuddsZfGSPA130_provenance; np:hasPublicationInfo dgn-np:NP1364241.RAZqaQ3QxVA_v6zdDuHIK30oed8tzsNF4QSuddsZfGSPA130_publicationInfo; a np:Nanopublication . dgn-np:NP1364241.RAZqaQ3QxVA_v6zdDuHIK30oed8tzsNF4QSuddsZfGSPA130_assertion a np:Assertion . dgn-np:NP1364241.RAZqaQ3QxVA_v6zdDuHIK30oed8tzsNF4QSuddsZfGSPA130_provenance a np:Provenance . dgn-np:NP1364241.RAZqaQ3QxVA_v6zdDuHIK30oed8tzsNF4QSuddsZfGSPA130_publicationInfo a np:PublicationInfo . } dgn-np:NP1364241.RAZqaQ3QxVA_v6zdDuHIK30oed8tzsNF4QSuddsZfGSPA130_assertion { miriam-gene:81539 a ncit:C16612 . lld:C1827820 a ncit:C7057 . dgn-gda:DGN37aa9d86cc1fe4b98dcdbe0182c71a2c sio:SIO_000628 miriam-gene:81539, lld:C1827820; a sio:SIO_001121 . } dgn-np:NP1364241.RAZqaQ3QxVA_v6zdDuHIK30oed8tzsNF4QSuddsZfGSPA130_provenance { dgn-np:NP1364241.RAZqaQ3QxVA_v6zdDuHIK30oed8tzsNF4QSuddsZfGSPA130_assertion dcterms:description "[Individuals who lacked the GSTM1 gene and possessed a NAT2 slow-acetylator genotype had a risk of developing malignant and nonmalignant pulmonary disorders that was approximately fivefold greater than that observed for those who had the GSTM1 gene and a NAT2 fast-acetylator genotype (OR = 5.1; 95% CI = 1.6-17.6); these individuals had a fourfold increased risk of developing nonmalignant pulmonary disorders (OR = 4.1; 95% CI = 1.1-17.2) and an eightfold increased risk of developing malignant mesothelioma (OR = 7.8; 95% CI = 1.4-78.7) when compared with the same reference group.]. 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:8961976; 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:NP1364241.RAZqaQ3QxVA_v6zdDuHIK30oed8tzsNF4QSuddsZfGSPA130_publicationInfo { this: dcterms:created "2016-05-13T12:52:04+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" . }