@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:NP880717.RA2BqGjRAHG2r97AhJaoRyC05HKqKFXiNjJ0JDU_u3gos130_head { this: np:hasAssertion dgn-np:NP880717.RA2BqGjRAHG2r97AhJaoRyC05HKqKFXiNjJ0JDU_u3gos130_assertion; np:hasProvenance dgn-np:NP880717.RA2BqGjRAHG2r97AhJaoRyC05HKqKFXiNjJ0JDU_u3gos130_provenance; np:hasPublicationInfo dgn-np:NP880717.RA2BqGjRAHG2r97AhJaoRyC05HKqKFXiNjJ0JDU_u3gos130_publicationInfo; a np:Nanopublication . dgn-np:NP880717.RA2BqGjRAHG2r97AhJaoRyC05HKqKFXiNjJ0JDU_u3gos130_assertion a np:Assertion . dgn-np:NP880717.RA2BqGjRAHG2r97AhJaoRyC05HKqKFXiNjJ0JDU_u3gos130_provenance a np:Provenance . dgn-np:NP880717.RA2BqGjRAHG2r97AhJaoRyC05HKqKFXiNjJ0JDU_u3gos130_publicationInfo a np:PublicationInfo . } dgn-np:NP880717.RA2BqGjRAHG2r97AhJaoRyC05HKqKFXiNjJ0JDU_u3gos130_assertion { miriam-gene:7515 a ncit:C16612 . lld:C1168401 a ncit:C7057 . dgn-gda:DGN7645746f5f4b781c5e8ea3b19d0387fb sio:SIO_000628 miriam-gene:7515, lld:C1168401; a sio:SIO_001122 . } dgn-np:NP880717.RA2BqGjRAHG2r97AhJaoRyC05HKqKFXiNjJ0JDU_u3gos130_provenance { dgn-np:NP880717.RA2BqGjRAHG2r97AhJaoRyC05HKqKFXiNjJ0JDU_u3gos130_assertion dcterms:description "[Genetic variants ERCC2 Lys751Gln (rs13181), ERCC2 Asp312Asn (rs1799793), XRCC1 Arg194Trp (rs1799782); XRCC1 Gln399Arg (rs25487), XRCC1 Arg280His (rs25489) and XRCC3 Thr241Met (rs861539) were analyzed in a primary study group comprising 169 patients with histologically confirmed HNSCC and 463 healthy control subjects.]. 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:21419115; 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:NP880717.RA2BqGjRAHG2r97AhJaoRyC05HKqKFXiNjJ0JDU_u3gos130_publicationInfo { this: dcterms:created "2016-05-13T12:48:23+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" . }