@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8> .
@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:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_head {
  this: np:hasAssertion dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_assertion;
    np:hasProvenance dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_provenance;
    np:hasPublicationInfo dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_assertion a np:Assertion .
  
  dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_provenance a np:Provenance .
  
  dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_assertion {
  miriam-gene:4683 a ncit:C16612 .
  
  lld:C0684249 a ncit:C7057 .
  
  dgn-gda:DGNab47c5a1be09f30f5c6f948d008ca70b sio:SIO_000628 miriam-gene:4683, lld:C0684249;
    a sio:SIO_001121 .
}

dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_provenance {
  dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_assertion dcterms:description
      "[Our results show that the genetic variation in XRCC1, XRCC3 and NBS1 influence lung cancer susceptibility among women, and that combinations of risk alleles in the two HR genes can enhance the effects.]. 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:17034901;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:37+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" .
}