@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP382461.RABmp5VWfY4QWXeafq5rmW2YuGh8_r1UUcNHwwTeLy-hc> .
@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:NP382461.RABmp5VWfY4QWXeafq5rmW2YuGh8_r1UUcNHwwTeLy-hc130_head {
  this: np:hasAssertion dgn-np:NP382461.RABmp5VWfY4QWXeafq5rmW2YuGh8_r1UUcNHwwTeLy-hc130_assertion;
    np:hasProvenance dgn-np:NP382461.RABmp5VWfY4QWXeafq5rmW2YuGh8_r1UUcNHwwTeLy-hc130_provenance;
    np:hasPublicationInfo dgn-np:NP382461.RABmp5VWfY4QWXeafq5rmW2YuGh8_r1UUcNHwwTeLy-hc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP382461.RABmp5VWfY4QWXeafq5rmW2YuGh8_r1UUcNHwwTeLy-hc130_assertion a np:Assertion .
  
  dgn-np:NP382461.RABmp5VWfY4QWXeafq5rmW2YuGh8_r1UUcNHwwTeLy-hc130_provenance a np:Provenance .
  
  dgn-np:NP382461.RABmp5VWfY4QWXeafq5rmW2YuGh8_r1UUcNHwwTeLy-hc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP382461.RABmp5VWfY4QWXeafq5rmW2YuGh8_r1UUcNHwwTeLy-hc130_assertion {
  miriam-gene:2072 a ncit:C16612 .
  
  lld:C0005684 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP382461.RABmp5VWfY4QWXeafq5rmW2YuGh8_r1UUcNHwwTeLy-hc130_provenance {
  dgn-np:NP382461.RABmp5VWfY4QWXeafq5rmW2YuGh8_r1UUcNHwwTeLy-hc130_assertion dcterms:description
      "[We evaluated the influence of common genetic variation in the NER pathway on bladder cancer risk by analyzing 22 single nucleotide polymorphisms (SNP) in seven NER genes (XPC, RAD23B, ERCC1, ERCC2, ERCC4, ERCC5, and ERCC6).]. 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:16537713;
    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:NP382461.RABmp5VWfY4QWXeafq5rmW2YuGh8_r1UUcNHwwTeLy-hc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:21+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}