@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP340520.RADlcwt-Qz9i6PPN0GT2BoYfPlhR8w5E_4hP7TKYvPxTE> .
@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:NP340520.RADlcwt-Qz9i6PPN0GT2BoYfPlhR8w5E_4hP7TKYvPxTE130_head {
  this: np:hasAssertion dgn-np:NP340520.RADlcwt-Qz9i6PPN0GT2BoYfPlhR8w5E_4hP7TKYvPxTE130_assertion;
    np:hasProvenance dgn-np:NP340520.RADlcwt-Qz9i6PPN0GT2BoYfPlhR8w5E_4hP7TKYvPxTE130_provenance;
    np:hasPublicationInfo dgn-np:NP340520.RADlcwt-Qz9i6PPN0GT2BoYfPlhR8w5E_4hP7TKYvPxTE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP340520.RADlcwt-Qz9i6PPN0GT2BoYfPlhR8w5E_4hP7TKYvPxTE130_assertion a np:Assertion .
  
  dgn-np:NP340520.RADlcwt-Qz9i6PPN0GT2BoYfPlhR8w5E_4hP7TKYvPxTE130_provenance a np:Provenance .
  
  dgn-np:NP340520.RADlcwt-Qz9i6PPN0GT2BoYfPlhR8w5E_4hP7TKYvPxTE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP340520.RADlcwt-Qz9i6PPN0GT2BoYfPlhR8w5E_4hP7TKYvPxTE130_assertion {
  miriam-gene:1545 a ncit:C16612 .
  
  lld:C2931456 a ncit:C7057 .
  
  dgn-gda:DGNeb5e450e038018bd09cf9ad590567dde sio:SIO_000628 miriam-gene:1545, lld:C2931456;
    a sio:SIO_001121 .
}

dgn-np:NP340520.RADlcwt-Qz9i6PPN0GT2BoYfPlhR8w5E_4hP7TKYvPxTE130_provenance {
  dgn-np:NP340520.RADlcwt-Qz9i6PPN0GT2BoYfPlhR8w5E_4hP7TKYvPxTE130_assertion dcterms:description
      "[To test the hypothesis that genetic polymorphisms in the CYP1B1 gene may associate with the risk for prostate cancer (CaP), we compared the allele, genotype, and haplotype frequencies of 13 single nucleotide polymorphisms (SNPs) of CYP1B1 among 159 hereditary prostate cancer (HPC) probands, 245 sporadic CaP cases, and 222 unaffected men.]. 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:14562027;
    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:NP340520.RADlcwt-Qz9i6PPN0GT2BoYfPlhR8w5E_4hP7TKYvPxTE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:56+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" .
}