@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:NP607957.RAVlvB2VzMiZzPcH-Jv271oCAAe85Vi_AJDFbJjk_nT48130_head { this: np:hasAssertion dgn-np:NP607957.RAVlvB2VzMiZzPcH-Jv271oCAAe85Vi_AJDFbJjk_nT48130_assertion; np:hasProvenance dgn-np:NP607957.RAVlvB2VzMiZzPcH-Jv271oCAAe85Vi_AJDFbJjk_nT48130_provenance; np:hasPublicationInfo dgn-np:NP607957.RAVlvB2VzMiZzPcH-Jv271oCAAe85Vi_AJDFbJjk_nT48130_publicationInfo; a np:Nanopublication . dgn-np:NP607957.RAVlvB2VzMiZzPcH-Jv271oCAAe85Vi_AJDFbJjk_nT48130_assertion a np:Assertion . dgn-np:NP607957.RAVlvB2VzMiZzPcH-Jv271oCAAe85Vi_AJDFbJjk_nT48130_provenance a np:Provenance . dgn-np:NP607957.RAVlvB2VzMiZzPcH-Jv271oCAAe85Vi_AJDFbJjk_nT48130_publicationInfo a np:PublicationInfo . } dgn-np:NP607957.RAVlvB2VzMiZzPcH-Jv271oCAAe85Vi_AJDFbJjk_nT48130_assertion { miriam-gene:7508 a ncit:C16612 . lld:C0043346 a ncit:C7057 . dgn-gda:DGN584feb11e789af7d8b43ba730ebd4032 sio:SIO_000628 miriam-gene:7508, lld:C0043346; a sio:SIO_001122 . } dgn-np:NP607957.RAVlvB2VzMiZzPcH-Jv271oCAAe85Vi_AJDFbJjk_nT48130_provenance { dgn-np:NP607957.RAVlvB2VzMiZzPcH-Jv271oCAAe85Vi_AJDFbJjk_nT48130_assertion dcterms:description "[We have studied 11 polymorphisms in genes of drug detoxification pathways (NQO1, glutathione S-transferase pi) and DNA repair xeroderma pigmentosum, complementation group (3) (XPC(3), X-ray repair cross complementing protein (1)), Nijmegen breakage syndrome (1), excision repair cross-complementing rodent repair deficiency, complementation group (5) and X-ray repair cross complementing protein (3) and in the methylene tetrahydrofolate reductase gene (MTHFR(2), 677C>T, 1298A>C), involved in DNA synthesis.]. 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:17476281; 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:NP607957.RAVlvB2VzMiZzPcH-Jv271oCAAe85Vi_AJDFbJjk_nT48130_publicationInfo { this: dcterms:created "2016-05-13T12:46:21+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" . }