@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP340318.RA0EzuVJININBXRw3m8bRYwsYdqz1mqVlySpcZFKr7iz8> .
@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:NP340318.RA0EzuVJININBXRw3m8bRYwsYdqz1mqVlySpcZFKr7iz8130_head {
  this: np:hasAssertion dgn-np:NP340318.RA0EzuVJININBXRw3m8bRYwsYdqz1mqVlySpcZFKr7iz8130_assertion;
    np:hasProvenance dgn-np:NP340318.RA0EzuVJININBXRw3m8bRYwsYdqz1mqVlySpcZFKr7iz8130_provenance;
    np:hasPublicationInfo dgn-np:NP340318.RA0EzuVJININBXRw3m8bRYwsYdqz1mqVlySpcZFKr7iz8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP340318.RA0EzuVJININBXRw3m8bRYwsYdqz1mqVlySpcZFKr7iz8130_assertion a np:Assertion .
  
  dgn-np:NP340318.RA0EzuVJININBXRw3m8bRYwsYdqz1mqVlySpcZFKr7iz8130_provenance a np:Provenance .
  
  dgn-np:NP340318.RA0EzuVJININBXRw3m8bRYwsYdqz1mqVlySpcZFKr7iz8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP340318.RA0EzuVJININBXRw3m8bRYwsYdqz1mqVlySpcZFKr7iz8130_assertion {
  miriam-gene:1545 a ncit:C16612 .
  
  lld:C0238339 a ncit:C7057 .
  
  dgn-gda:DGN4d5f53ae137ab49a9119be9cd6c6299f sio:SIO_000628 miriam-gene:1545, lld:C0238339;
    a sio:SIO_001121 .
}

dgn-np:NP340318.RA0EzuVJININBXRw3m8bRYwsYdqz1mqVlySpcZFKr7iz8130_provenance {
  dgn-np:NP340318.RA0EzuVJININBXRw3m8bRYwsYdqz1mqVlySpcZFKr7iz8130_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:NP340318.RA0EzuVJININBXRw3m8bRYwsYdqz1mqVlySpcZFKr7iz8130_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" .
}