@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:NP46104.RA6eNiNiex2fvJjownaRDIKCD1WwhJiyWz1zs9BeJqFPE130_head { this: np:hasAssertion dgn-np:NP46104.RA6eNiNiex2fvJjownaRDIKCD1WwhJiyWz1zs9BeJqFPE130_assertion; np:hasProvenance dgn-np:NP46104.RA6eNiNiex2fvJjownaRDIKCD1WwhJiyWz1zs9BeJqFPE130_provenance; np:hasPublicationInfo dgn-np:NP46104.RA6eNiNiex2fvJjownaRDIKCD1WwhJiyWz1zs9BeJqFPE130_publicationInfo; a np:Nanopublication . dgn-np:NP46104.RA6eNiNiex2fvJjownaRDIKCD1WwhJiyWz1zs9BeJqFPE130_assertion a np:Assertion . dgn-np:NP46104.RA6eNiNiex2fvJjownaRDIKCD1WwhJiyWz1zs9BeJqFPE130_provenance a np:Provenance . dgn-np:NP46104.RA6eNiNiex2fvJjownaRDIKCD1WwhJiyWz1zs9BeJqFPE130_publicationInfo a np:PublicationInfo . } dgn-np:NP46104.RA6eNiNiex2fvJjownaRDIKCD1WwhJiyWz1zs9BeJqFPE130_assertion { miriam-gene:1543 a ncit:C16612 . lld:C0242379 a ncit:C7057 . dgn-gda:DGN89607cbae4141fde20c6067cc8f235e1 sio:SIO_000628 miriam-gene:1543, lld:C0242379; a sio:SIO_001122 . } dgn-np:NP46104.RA6eNiNiex2fvJjownaRDIKCD1WwhJiyWz1zs9BeJqFPE130_provenance { dgn-np:NP46104.RA6eNiNiex2fvJjownaRDIKCD1WwhJiyWz1zs9BeJqFPE130_assertion dcterms:description "[Through a systematic literature search for publications between 1989 and 2006, we summarized the data from 46 studies on polymorphisms of MspI and exon7-Val of CYP1A1 and GSTM1 and lung cancer risk in Chinese populations, and found that compared with the wild-type homozygous genotype (type A), lung cancer risk for the combined variant genotypes (types B and C) was 1.34-fold (95% confidence interval CI=1.08-1.67) (Z=2.64, P=0.008); the risk for the combined variant genotypes (Ile/Val and Val/Val) of CYP1A1 exon7 was 1.61-fold (95% CI=1.24-2.08) (Z=3.62, P<0.001), compared with the Ile/Ile genotype; and that the risk for the GSTM1 null genotype was 1.54-fold (95% CI=1.31-1.80) (Z=5.32, P<0.001), compared with the GSTM1 present genotype.]. 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:17900751; prov:wasDerivedFrom dgn-void:gad-20130706; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP46104.RA6eNiNiex2fvJjownaRDIKCD1WwhJiyWz1zs9BeJqFPE130_publicationInfo { this: dcterms:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }