@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45932.RAKdi4Edn4r4MVPkDw3r6hq7AvjgZQHKGzDMWwH2iRzgU> .
@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:NP45932.RAKdi4Edn4r4MVPkDw3r6hq7AvjgZQHKGzDMWwH2iRzgU130_head {
  this: np:hasAssertion dgn-np:NP45932.RAKdi4Edn4r4MVPkDw3r6hq7AvjgZQHKGzDMWwH2iRzgU130_assertion;
    np:hasProvenance dgn-np:NP45932.RAKdi4Edn4r4MVPkDw3r6hq7AvjgZQHKGzDMWwH2iRzgU130_provenance;
    np:hasPublicationInfo dgn-np:NP45932.RAKdi4Edn4r4MVPkDw3r6hq7AvjgZQHKGzDMWwH2iRzgU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45932.RAKdi4Edn4r4MVPkDw3r6hq7AvjgZQHKGzDMWwH2iRzgU130_assertion a np:Assertion .
  
  dgn-np:NP45932.RAKdi4Edn4r4MVPkDw3r6hq7AvjgZQHKGzDMWwH2iRzgU130_provenance a np:Provenance .
  
  dgn-np:NP45932.RAKdi4Edn4r4MVPkDw3r6hq7AvjgZQHKGzDMWwH2iRzgU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45932.RAKdi4Edn4r4MVPkDw3r6hq7AvjgZQHKGzDMWwH2iRzgU130_assertion {
  miriam-gene:1545 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN2a9856cd17b1ac994055e1ca142c44b3 sio:SIO_000628 miriam-gene:1545, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP45932.RAKdi4Edn4r4MVPkDw3r6hq7AvjgZQHKGzDMWwH2iRzgU130_provenance {
  dgn-np:NP45932.RAKdi4Edn4r4MVPkDw3r6hq7AvjgZQHKGzDMWwH2iRzgU130_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: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:NP45932.RAKdi4Edn4r4MVPkDw3r6hq7AvjgZQHKGzDMWwH2iRzgU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}