@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:NP118938.RAXso7koESFxV7KFXGAD9h0QeCUhLp_aPyYPBoYheM3Ss130_head { this: np:hasAssertion dgn-np:NP118938.RAXso7koESFxV7KFXGAD9h0QeCUhLp_aPyYPBoYheM3Ss130_assertion; np:hasProvenance dgn-np:NP118938.RAXso7koESFxV7KFXGAD9h0QeCUhLp_aPyYPBoYheM3Ss130_provenance; np:hasPublicationInfo dgn-np:NP118938.RAXso7koESFxV7KFXGAD9h0QeCUhLp_aPyYPBoYheM3Ss130_publicationInfo; a np:Nanopublication . dgn-np:NP118938.RAXso7koESFxV7KFXGAD9h0QeCUhLp_aPyYPBoYheM3Ss130_assertion a np:Assertion . dgn-np:NP118938.RAXso7koESFxV7KFXGAD9h0QeCUhLp_aPyYPBoYheM3Ss130_provenance a np:Provenance . dgn-np:NP118938.RAXso7koESFxV7KFXGAD9h0QeCUhLp_aPyYPBoYheM3Ss130_publicationInfo a np:PublicationInfo . } dgn-np:NP118938.RAXso7koESFxV7KFXGAD9h0QeCUhLp_aPyYPBoYheM3Ss130_assertion { miriam-gene:3586 a ncit:C16612 . lld:C0007137 a ncit:C7057 . dgn-gda:DGN003b16b8adf3ddcd8e99dd7da888bf77 sio:SIO_000628 miriam-gene:3586, lld:C0007137; a sio:SIO_001122 . } dgn-np:NP118938.RAXso7koESFxV7KFXGAD9h0QeCUhLp_aPyYPBoYheM3Ss130_provenance { dgn-np:NP118938.RAXso7koESFxV7KFXGAD9h0QeCUhLp_aPyYPBoYheM3Ss130_assertion dcterms:description "[Furthermore, when the mode of inheritance of each variant allele was taken into account in a biological multivariate logistic regression model, four polymorphisms emerged as primary predictors for overall stages of OSCC: TNF-alpha (OR = 15.27; 95% CI = 7.30-31.96), IL-6 (OR = 8.33; 95% CI = 3.95-17.58), IL-8 (OR = 3.54; 95% CI = 1.69-7.43) and IL-10 (OR = 2.65; 95% CI = 1.28-5.46).]. 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:18273643; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP118938.RAXso7koESFxV7KFXGAD9h0QeCUhLp_aPyYPBoYheM3Ss130_publicationInfo { this: dcterms:created "2016-05-13T12:42:41+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" . }