@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP967467.RADM7ybzIE8uoZ6P_uMTrOUW_VX94b3rqn7BMvpAtiZyk> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP967467.RADM7ybzIE8uoZ6P_uMTrOUW_VX94b3rqn7BMvpAtiZyk130_head {
   this: np:hasAssertion dgn-np:NP967467.RADM7ybzIE8uoZ6P_uMTrOUW_VX94b3rqn7BMvpAtiZyk130_assertion ;
    np:hasProvenance dgn-np:NP967467.RADM7ybzIE8uoZ6P_uMTrOUW_VX94b3rqn7BMvpAtiZyk130_provenance ;
    np:hasPublicationInfo dgn-np:NP967467.RADM7ybzIE8uoZ6P_uMTrOUW_VX94b3rqn7BMvpAtiZyk130_publicationInfo ;
    a np:Nanopublication .
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}
dgn-np:NP967467.RADM7ybzIE8uoZ6P_uMTrOUW_VX94b3rqn7BMvpAtiZyk130_assertion {
   miriam-gene:121227 a ncit:C16612 .
  lld:C0005684 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP967467.RADM7ybzIE8uoZ6P_uMTrOUW_VX94b3rqn7BMvpAtiZyk130_provenance {
   dgn-np:NP967467.RADM7ybzIE8uoZ6P_uMTrOUW_VX94b3rqn7BMvpAtiZyk130_assertion dcterms:description "[In order to examine the association of common genetic variation in the base-excision repair (BER) pathway with bladder cancer risk, we analyzed 43 single nucleotide polymorphisms (SNPs) in 12 BER genes (OGG1, MUTYH, APEX1, PARP1, PARP3, PARP4, XRCC1, POLB, POLD1, PCNA, LIG1, and LIG3).]. 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:17203305 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
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  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:NP967467.RADM7ybzIE8uoZ6P_uMTrOUW_VX94b3rqn7BMvpAtiZyk130_publicationInfo {
   this: dcterms:created "2015-08-25T14:47:31+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
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