@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63639.RAfLxHPoeX1DJPaRTX3e28bAbjrptRxbLiPVDJWTP42t4> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP63639.RAfLxHPoeX1DJPaRTX3e28bAbjrptRxbLiPVDJWTP42t4130_head {
  this: np:hasAssertion dgn-np:NP63639.RAfLxHPoeX1DJPaRTX3e28bAbjrptRxbLiPVDJWTP42t4130_assertion;
    np:hasProvenance dgn-np:NP63639.RAfLxHPoeX1DJPaRTX3e28bAbjrptRxbLiPVDJWTP42t4130_provenance;
    np:hasPublicationInfo dgn-np:NP63639.RAfLxHPoeX1DJPaRTX3e28bAbjrptRxbLiPVDJWTP42t4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP63639.RAfLxHPoeX1DJPaRTX3e28bAbjrptRxbLiPVDJWTP42t4130_assertion a np:Assertion .
  
  dgn-np:NP63639.RAfLxHPoeX1DJPaRTX3e28bAbjrptRxbLiPVDJWTP42t4130_provenance a np:Provenance .
  
  dgn-np:NP63639.RAfLxHPoeX1DJPaRTX3e28bAbjrptRxbLiPVDJWTP42t4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP63639.RAfLxHPoeX1DJPaRTX3e28bAbjrptRxbLiPVDJWTP42t4130_assertion {
  miriam-gene:328 a ncit:C16612 .
  
  lld:C0005684 a ncit:C7057 .
  
  dgn-gda:DGN4a776e970c583f4158b5a469149e205d sio:SIO_000628 miriam-gene:328, lld:C0005684;
    a sio:SIO_001122 .
}

dgn-np:NP63639.RAfLxHPoeX1DJPaRTX3e28bAbjrptRxbLiPVDJWTP42t4130_provenance {
  dgn-np:NP63639.RAfLxHPoeX1DJPaRTX3e28bAbjrptRxbLiPVDJWTP42t4130_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:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP63639.RAfLxHPoeX1DJPaRTX3e28bAbjrptRxbLiPVDJWTP42t4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    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>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}