@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I> .
@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:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_head {
  this: np:hasAssertion dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_assertion;
    np:hasProvenance dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_provenance;
    np:hasPublicationInfo dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_assertion a np:Assertion .
  
  dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_provenance a np:Provenance .
  
  dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_assertion {
  miriam-gene:1234 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN22e83dfcb9045dcc3e868124b449cc50 sio:SIO_000628 miriam-gene:1234, lld:C0376358;
    a sio:SIO_001121 .
}

dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_provenance {
  dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_assertion dcterms:description
      "[Our data indicate that gene polymorphism of CCR2 V64I may influence the susceptibility and clinicopathological characteristics of prostate cancer and CCR5 Δ32 allele may also be an important risk factor for prostate cancer in Turkish men population.]. 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:22612293;
    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:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:09+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" .
}