@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:NP919049.RAlw7OeLJrZzwhlgc2BLAvJO-m37OcYdQz4kJr2j123Zk130_head { this: np:hasAssertion dgn-np:NP919049.RAlw7OeLJrZzwhlgc2BLAvJO-m37OcYdQz4kJr2j123Zk130_assertion; np:hasProvenance dgn-np:NP919049.RAlw7OeLJrZzwhlgc2BLAvJO-m37OcYdQz4kJr2j123Zk130_provenance; np:hasPublicationInfo dgn-np:NP919049.RAlw7OeLJrZzwhlgc2BLAvJO-m37OcYdQz4kJr2j123Zk130_publicationInfo; a np:Nanopublication . dgn-np:NP919049.RAlw7OeLJrZzwhlgc2BLAvJO-m37OcYdQz4kJr2j123Zk130_assertion a np:Assertion . dgn-np:NP919049.RAlw7OeLJrZzwhlgc2BLAvJO-m37OcYdQz4kJr2j123Zk130_provenance a np:Provenance . dgn-np:NP919049.RAlw7OeLJrZzwhlgc2BLAvJO-m37OcYdQz4kJr2j123Zk130_publicationInfo a np:PublicationInfo . } dgn-np:NP919049.RAlw7OeLJrZzwhlgc2BLAvJO-m37OcYdQz4kJr2j123Zk130_assertion { miriam-gene:7515 a ncit:C16612 . lld:C0019163 a ncit:C7057 . dgn-gda:DGNbbd667ae543926391ebfdc025980c763 sio:SIO_000628 miriam-gene:7515, lld:C0019163; a sio:SIO_001121 . } dgn-np:NP919049.RAlw7OeLJrZzwhlgc2BLAvJO-m37OcYdQz4kJr2j123Zk130_provenance { dgn-np:NP919049.RAlw7OeLJrZzwhlgc2BLAvJO-m37OcYdQz4kJr2j123Zk130_assertion dcterms:description "[Sensitivity analysis further showed that there was no association between XRCC1 Arg399Gln polymorphism and risk of hepatitis B-related hepatocellular carcinoma under all contrast models (Gln vs. Arg: fixed-effect OR = 0.93, 95 % CI 0.82-1.05, P = 0.25; GlnGln vs. ArgArg: fixed-effect OR = 0.86, 95 % CI 0.64-1.16, P = 0.32; GlnGln/ArgGln vs. ArgArg: fixed-effect OR = 0.93, 95 % CI 0.80-1.10, P = 0.41; and GlnGln vs. ArgArg/ArgGln: fixed-effect OR = 0.85, 95 % CI 0.63-1.13, P = 0.26).]. 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:23780894; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP919049.RAlw7OeLJrZzwhlgc2BLAvJO-m37OcYdQz4kJr2j123Zk130_publicationInfo { this: dcterms:created "2014-10-02T12:41:24+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" . }