@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:NP972554.RA--73pTwET0lw3uW8MC4W51hMq1QJQOM3Og4NV8Kv0bU130_head { this: np:hasAssertion dgn-np:NP972554.RA--73pTwET0lw3uW8MC4W51hMq1QJQOM3Og4NV8Kv0bU130_assertion; np:hasProvenance dgn-np:NP972554.RA--73pTwET0lw3uW8MC4W51hMq1QJQOM3Og4NV8Kv0bU130_provenance; np:hasPublicationInfo dgn-np:NP972554.RA--73pTwET0lw3uW8MC4W51hMq1QJQOM3Og4NV8Kv0bU130_publicationInfo; a np:Nanopublication . dgn-np:NP972554.RA--73pTwET0lw3uW8MC4W51hMq1QJQOM3Og4NV8Kv0bU130_assertion a np:Assertion . dgn-np:NP972554.RA--73pTwET0lw3uW8MC4W51hMq1QJQOM3Og4NV8Kv0bU130_provenance a np:Provenance . dgn-np:NP972554.RA--73pTwET0lw3uW8MC4W51hMq1QJQOM3Og4NV8Kv0bU130_publicationInfo a np:PublicationInfo . } dgn-np:NP972554.RA--73pTwET0lw3uW8MC4W51hMq1QJQOM3Og4NV8Kv0bU130_assertion { miriam-gene:2950 a ncit:C16612 . lld:C0019829 a ncit:C7057 . dgn-gda:DGNe50d28b44d511df17f955d49b6b4426e sio:SIO_000628 miriam-gene:2950, lld:C0019829; a sio:SIO_001122 . } dgn-np:NP972554.RA--73pTwET0lw3uW8MC4W51hMq1QJQOM3Og4NV8Kv0bU130_provenance { dgn-np:NP972554.RA--73pTwET0lw3uW8MC4W51hMq1QJQOM3Og4NV8Kv0bU130_assertion dcterms:description "[The GSTP1 rs1695 A-allele reduced the risk for HL (GG vs. AG, OR 0.64 [0.42-0.99], p = 0.04; GG vs. AG/AA combined genotypes, OR 0.70 [0.47-1.04], p = 0.07), and the GSTT1 deleted genotype increased the risk for HL (OR 3.17 [1.97-5.09], p < 0.001) regardless of age.]. 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:22475179; 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:NP972554.RA--73pTwET0lw3uW8MC4W51hMq1QJQOM3Og4NV8Kv0bU130_publicationInfo { this: dcterms:created "2016-05-13T12:49:05+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" . }