@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:NP438993.RA5hl7mOu3JR_XOvcJZ6VCB5msdiVZzzLfZQlzZSpMvSw130_head { this: np:hasAssertion dgn-np:NP438993.RA5hl7mOu3JR_XOvcJZ6VCB5msdiVZzzLfZQlzZSpMvSw130_assertion; np:hasProvenance dgn-np:NP438993.RA5hl7mOu3JR_XOvcJZ6VCB5msdiVZzzLfZQlzZSpMvSw130_provenance; np:hasPublicationInfo dgn-np:NP438993.RA5hl7mOu3JR_XOvcJZ6VCB5msdiVZzzLfZQlzZSpMvSw130_publicationInfo; a np:Nanopublication . dgn-np:NP438993.RA5hl7mOu3JR_XOvcJZ6VCB5msdiVZzzLfZQlzZSpMvSw130_assertion a np:Assertion . dgn-np:NP438993.RA5hl7mOu3JR_XOvcJZ6VCB5msdiVZzzLfZQlzZSpMvSw130_provenance a np:Provenance . dgn-np:NP438993.RA5hl7mOu3JR_XOvcJZ6VCB5msdiVZzzLfZQlzZSpMvSw130_publicationInfo a np:PublicationInfo . } dgn-np:NP438993.RA5hl7mOu3JR_XOvcJZ6VCB5msdiVZzzLfZQlzZSpMvSw130_assertion { miriam-gene:2947 a ncit:C16612 . lld:C0007107 a ncit:C7057 . dgn-gda:DGN8896161d499d5cbe8b5e6114e277633f sio:SIO_000628 miriam-gene:2947, lld:C0007107; a sio:SIO_001121 . } dgn-np:NP438993.RA5hl7mOu3JR_XOvcJZ6VCB5msdiVZzzLfZQlzZSpMvSw130_provenance { dgn-np:NP438993.RA5hl7mOu3JR_XOvcJZ6VCB5msdiVZzzLfZQlzZSpMvSw130_assertion dcterms:description "[Stratification by tumor site indicated that the GSTM3 polymorphism was associated with a decreased risk of laryngeal cancer under recessive model and homozygote comparison (OR = 0.52, 95%CI: 0.30-0.89; and OR = 0.50, 95%CI: 0.29-0.87, respectively); By stratifying source of control, decreased cancer risk was observed in hospital-based population under all genetic models (OR = 0.67, 95%CI: 0.56-0.81 for the dominant model; OR = 0.66, 95%CI: 0.46-0.95 for the recessive model; OR = 0.55, 95%CI: 0.37-0.83 for the homozygote comparison model, and OR = 0.70, 95%CI: 0.58-0.84 for the heterozygote comparison model).]. 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:24416175; 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:NP438993.RA5hl7mOu3JR_XOvcJZ6VCB5msdiVZzzLfZQlzZSpMvSw130_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" . }