@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59404.RAuIrPqxo_z9P8Z1JlM0yQjlTiIaxwBvZUhNsgM1fNQkw> .
@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:NP59404.RAuIrPqxo_z9P8Z1JlM0yQjlTiIaxwBvZUhNsgM1fNQkw130_head {
  this: np:hasAssertion dgn-np:NP59404.RAuIrPqxo_z9P8Z1JlM0yQjlTiIaxwBvZUhNsgM1fNQkw130_assertion;
    np:hasProvenance dgn-np:NP59404.RAuIrPqxo_z9P8Z1JlM0yQjlTiIaxwBvZUhNsgM1fNQkw130_provenance;
    np:hasPublicationInfo dgn-np:NP59404.RAuIrPqxo_z9P8Z1JlM0yQjlTiIaxwBvZUhNsgM1fNQkw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59404.RAuIrPqxo_z9P8Z1JlM0yQjlTiIaxwBvZUhNsgM1fNQkw130_assertion a np:Assertion .
  
  dgn-np:NP59404.RAuIrPqxo_z9P8Z1JlM0yQjlTiIaxwBvZUhNsgM1fNQkw130_provenance a np:Provenance .
  
  dgn-np:NP59404.RAuIrPqxo_z9P8Z1JlM0yQjlTiIaxwBvZUhNsgM1fNQkw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59404.RAuIrPqxo_z9P8Z1JlM0yQjlTiIaxwBvZUhNsgM1fNQkw130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  
  lld:C0005684 a ncit:C7057 .
  
  dgn-gda:DGN8edbe68dbe5b8e5308e4eaf0019fcf34 sio:SIO_000628 miriam-gene:7515, lld:C0005684;
    a sio:SIO_001122 .
}

dgn-np:NP59404.RAuIrPqxo_z9P8Z1JlM0yQjlTiIaxwBvZUhNsgM1fNQkw130_provenance {
  dgn-np:NP59404.RAuIrPqxo_z9P8Z1JlM0yQjlTiIaxwBvZUhNsgM1fNQkw130_assertion dcterms:description
      "[We provide no evidence of an association between polymorphisms in XRCC1 and bladder cancer risk, although our study had only limited power to detect the association for low frequency variants, such as Arg280His.]. 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:17425776;
    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:NP59404.RAuIrPqxo_z9P8Z1JlM0yQjlTiIaxwBvZUhNsgM1fNQkw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}