@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:NP705157.RApLZKnbv97sM7Uynl7RAol5-fw3g-vuvAxtZw1i2EQoc130_head { this: np:hasAssertion dgn-np:NP705157.RApLZKnbv97sM7Uynl7RAol5-fw3g-vuvAxtZw1i2EQoc130_assertion; np:hasProvenance dgn-np:NP705157.RApLZKnbv97sM7Uynl7RAol5-fw3g-vuvAxtZw1i2EQoc130_provenance; np:hasPublicationInfo dgn-np:NP705157.RApLZKnbv97sM7Uynl7RAol5-fw3g-vuvAxtZw1i2EQoc130_publicationInfo; a np:Nanopublication . dgn-np:NP705157.RApLZKnbv97sM7Uynl7RAol5-fw3g-vuvAxtZw1i2EQoc130_assertion a np:Assertion . dgn-np:NP705157.RApLZKnbv97sM7Uynl7RAol5-fw3g-vuvAxtZw1i2EQoc130_provenance a np:Provenance . dgn-np:NP705157.RApLZKnbv97sM7Uynl7RAol5-fw3g-vuvAxtZw1i2EQoc130_publicationInfo a np:PublicationInfo . } dgn-np:NP705157.RApLZKnbv97sM7Uynl7RAol5-fw3g-vuvAxtZw1i2EQoc130_assertion { miriam-gene:7515 a ncit:C16612 . lld:C0043346 a ncit:C7057 . dgn-gda:DGN0a20038e211a5b7db8f862441fae3716 sio:SIO_000628 miriam-gene:7515, lld:C0043346; a sio:SIO_001121 . } dgn-np:NP705157.RApLZKnbv97sM7Uynl7RAol5-fw3g-vuvAxtZw1i2EQoc130_provenance { dgn-np:NP705157.RApLZKnbv97sM7Uynl7RAol5-fw3g-vuvAxtZw1i2EQoc130_assertion dcterms:description "[We analyzed 13 polymorphisms in seven DNA repair genes belonging to different repair pathways [X-ray repair cross-complementing group 1 (XRCC1): 26304C>T, 26651A>G, 28152A>G; xeroderma pigmentosum-D (XPD): 23591A>G, 35931A>C; excision repair complementing defective in Chinese hamster, group 1 (ERCC1): 19007C>T; XRCC3: 4541T>C, 17893A>G, 18067C>T; proliferating cell nuclear antigen (PCNA): 6084G>C; ERCC4: 30028C>T, 30147A>G; and XRCC2-31479A>G] in 317 incident bladder cancer patients and 317 controls.]. 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:16284380; 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:NP705157.RApLZKnbv97sM7Uynl7RAol5-fw3g-vuvAxtZw1i2EQoc130_publicationInfo { this: dcterms:created "2014-10-02T12:39:08+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" . }