@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:NP602390.RAOKTbF7gQxrbDlhq8KC3sExmxb2P22l4we1uOWKWeoKU130_head { this: np:hasAssertion dgn-np:NP602390.RAOKTbF7gQxrbDlhq8KC3sExmxb2P22l4we1uOWKWeoKU130_assertion; np:hasProvenance dgn-np:NP602390.RAOKTbF7gQxrbDlhq8KC3sExmxb2P22l4we1uOWKWeoKU130_provenance; np:hasPublicationInfo dgn-np:NP602390.RAOKTbF7gQxrbDlhq8KC3sExmxb2P22l4we1uOWKWeoKU130_publicationInfo; a np:Nanopublication . dgn-np:NP602390.RAOKTbF7gQxrbDlhq8KC3sExmxb2P22l4we1uOWKWeoKU130_assertion a np:Assertion . dgn-np:NP602390.RAOKTbF7gQxrbDlhq8KC3sExmxb2P22l4we1uOWKWeoKU130_provenance a np:Provenance . dgn-np:NP602390.RAOKTbF7gQxrbDlhq8KC3sExmxb2P22l4we1uOWKWeoKU130_publicationInfo a np:PublicationInfo . } dgn-np:NP602390.RAOKTbF7gQxrbDlhq8KC3sExmxb2P22l4we1uOWKWeoKU130_assertion { miriam-gene:4968 a ncit:C16612 . lld:C1883486 a ncit:C7057 . dgn-gda:DGN4a6655a023560d20503b1655399b28cd sio:SIO_000628 miriam-gene:4968, lld:C1883486; a sio:SIO_001121 . } dgn-np:NP602390.RAOKTbF7gQxrbDlhq8KC3sExmxb2P22l4we1uOWKWeoKU130_provenance { dgn-np:NP602390.RAOKTbF7gQxrbDlhq8KC3sExmxb2P22l4we1uOWKWeoKU130_assertion dcterms:description "[Given the crucial role of the APEX and OGG1 proteins in BER of oxidative DNA damage, the identified polymorphisms are good candidates for genetic epidemiologic studies of cancer susceptibility, while the finding that three of 20 (15%) endometrial tumors have somatic mutations in APEX suggests that inactivation of the BER pathway is important for the development of endometrial cancer in at least a subset of cases.]. 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:11465542; 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:NP602390.RAOKTbF7gQxrbDlhq8KC3sExmxb2P22l4we1uOWKWeoKU130_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" . }