@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:NP602345.RAC8dUVX99q4Bdn3GrGfzYggQ8tw6cwS9cYjIcanSZbaM130_head { this: np:hasAssertion dgn-np:NP602345.RAC8dUVX99q4Bdn3GrGfzYggQ8tw6cwS9cYjIcanSZbaM130_assertion; np:hasProvenance dgn-np:NP602345.RAC8dUVX99q4Bdn3GrGfzYggQ8tw6cwS9cYjIcanSZbaM130_provenance; np:hasPublicationInfo dgn-np:NP602345.RAC8dUVX99q4Bdn3GrGfzYggQ8tw6cwS9cYjIcanSZbaM130_publicationInfo; a np:Nanopublication . dgn-np:NP602345.RAC8dUVX99q4Bdn3GrGfzYggQ8tw6cwS9cYjIcanSZbaM130_assertion a np:Assertion . dgn-np:NP602345.RAC8dUVX99q4Bdn3GrGfzYggQ8tw6cwS9cYjIcanSZbaM130_provenance a np:Provenance . dgn-np:NP602345.RAC8dUVX99q4Bdn3GrGfzYggQ8tw6cwS9cYjIcanSZbaM130_publicationInfo a np:PublicationInfo . } dgn-np:NP602345.RAC8dUVX99q4Bdn3GrGfzYggQ8tw6cwS9cYjIcanSZbaM130_assertion { miriam-gene:4968 a ncit:C16612 . lld:C0746102 a ncit:C7057 . dgn-gda:DGNbf28388040e2ae850a9dc911b6b008a9 sio:SIO_000628 miriam-gene:4968, lld:C0746102; a sio:SIO_001121 . } dgn-np:NP602345.RAC8dUVX99q4Bdn3GrGfzYggQ8tw6cwS9cYjIcanSZbaM130_provenance { dgn-np:NP602345.RAC8dUVX99q4Bdn3GrGfzYggQ8tw6cwS9cYjIcanSZbaM130_assertion dcterms:description "[Overall, the hOGG1 genotype was not significantly associated with HCC; adjusted odds ratios (and 95% confidence intervals) for the Ser/Cys and Cys/Cys genotypes compared with the Ser/Ser genotype were 0.79 (0.35-1.79) and 0.48 (0.18-1.27) against hospital controls, and 1.51 (0.96-3.37) and 0.86 (0.50-1.47) against CLD patients.]. 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:17085873; 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:NP602345.RAC8dUVX99q4Bdn3GrGfzYggQ8tw6cwS9cYjIcanSZbaM130_publicationInfo { this: dcterms:created "2015-08-25T14:43:40+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" . }