@prefix orcid: . @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:NP257298.RAi6DfmNARt45jBWBIrufd09TH5psl4daE76V4KaF9p2Y130_head { this: np:hasAssertion dgn-np:NP257298.RAi6DfmNARt45jBWBIrufd09TH5psl4daE76V4KaF9p2Y130_assertion; np:hasProvenance dgn-np:NP257298.RAi6DfmNARt45jBWBIrufd09TH5psl4daE76V4KaF9p2Y130_provenance; np:hasPublicationInfo dgn-np:NP257298.RAi6DfmNARt45jBWBIrufd09TH5psl4daE76V4KaF9p2Y130_publicationInfo; a np:Nanopublication . dgn-np:NP257298.RAi6DfmNARt45jBWBIrufd09TH5psl4daE76V4KaF9p2Y130_assertion a np:Assertion . dgn-np:NP257298.RAi6DfmNARt45jBWBIrufd09TH5psl4daE76V4KaF9p2Y130_provenance a np:Provenance . dgn-np:NP257298.RAi6DfmNARt45jBWBIrufd09TH5psl4daE76V4KaF9p2Y130_publicationInfo a np:PublicationInfo . } dgn-np:NP257298.RAi6DfmNARt45jBWBIrufd09TH5psl4daE76V4KaF9p2Y130_assertion { miriam-gene:545 a ncit:C16612 . lld:C0007131 a ncit:C7057 . dgn-gda:DGN3c2320e884143f554aa48b31e95a7eec sio:SIO_000628 miriam-gene:545, lld:C0007131; a sio:SIO_001122 . } dgn-np:NP257298.RAi6DfmNARt45jBWBIrufd09TH5psl4daE76V4KaF9p2Y130_provenance { dgn-np:NP257298.RAi6DfmNARt45jBWBIrufd09TH5psl4daE76V4KaF9p2Y130_assertion dcterms:description "[Our results indicate that SNPs in the NER genes ERCC1 (Asn118Asn, 15310G>C, 8902G>T), XPA (-4G>A), ERCC2/XPD (Lys751Gln) and ERCC5/XPD (His46His); the BER genes APE1/APEX (Ile64Val), OGG1 (Ser326Cys), PCNA (1876A>G) and XRCC1 (Arg194Trp, Arg280His, Arg399Gln); and the DSB-R genes ATR (Thr211Met), NBS1 (Glu185Gln), XRCC2 (Arg188His) and XRCC9 (Thr297Ile) modulate NSCLC risk.]. 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:16195237; 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:NP257298.RAi6DfmNARt45jBWBIrufd09TH5psl4daE76V4KaF9p2Y130_publicationInfo { this: dcterms:created "2015-08-25T14:40:06+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X, orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654; pav:createdBy orcid:0000-0003-0169-8159; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }