@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc> .
@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:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_head {
  this: np:hasAssertion dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_assertion;
    np:hasProvenance dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_provenance;
    np:hasPublicationInfo dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_assertion a np:Assertion .
  
  dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_provenance a np:Provenance .
  
  dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  
  lld:C0005684 a ncit:C7057 .
  
  dgn-gda:DGN4bf2db64781344bedef54dafa5c9915b sio:SIO_000628 miriam-gene:7515, lld:C0005684;
    a sio:SIO_001122 .
}

dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_provenance {
  dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_assertion dcterms:description
      "[It indicated that XRCC1 R399Q and R194W might not be risk factors to bladder cancer, but the 399QQ genotype decreased susceptibility of bladder cancer under recessive model and homozygote contrast among ever-smokers.]. 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:18765423;
    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:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_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" .
}