@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58986.RABqjqAcC_qpCbKXYTjmgfJx4_A92uH3AaV0lDkW3FPKk> .
@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:NP58986.RABqjqAcC_qpCbKXYTjmgfJx4_A92uH3AaV0lDkW3FPKk130_head {
  this: np:hasAssertion dgn-np:NP58986.RABqjqAcC_qpCbKXYTjmgfJx4_A92uH3AaV0lDkW3FPKk130_assertion;
    np:hasProvenance dgn-np:NP58986.RABqjqAcC_qpCbKXYTjmgfJx4_A92uH3AaV0lDkW3FPKk130_provenance;
    np:hasPublicationInfo dgn-np:NP58986.RABqjqAcC_qpCbKXYTjmgfJx4_A92uH3AaV0lDkW3FPKk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58986.RABqjqAcC_qpCbKXYTjmgfJx4_A92uH3AaV0lDkW3FPKk130_assertion a np:Assertion .
  
  dgn-np:NP58986.RABqjqAcC_qpCbKXYTjmgfJx4_A92uH3AaV0lDkW3FPKk130_provenance a np:Provenance .
  
  dgn-np:NP58986.RABqjqAcC_qpCbKXYTjmgfJx4_A92uH3AaV0lDkW3FPKk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58986.RABqjqAcC_qpCbKXYTjmgfJx4_A92uH3AaV0lDkW3FPKk130_assertion {
  miriam-gene:7421 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN1e2fd76da781ddc29419d6275f6b2b54 sio:SIO_000628 miriam-gene:7421, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP58986.RABqjqAcC_qpCbKXYTjmgfJx4_A92uH3AaV0lDkW3FPKk130_provenance {
  dgn-np:NP58986.RABqjqAcC_qpCbKXYTjmgfJx4_A92uH3AaV0lDkW3FPKk130_assertion dcterms:description
      "[The genotype frequencies for the three polymorphisms of the VDR gene within subgroups of PCa (defined by tumor stage, Gleason score, PSA levels) were also analyzed, but no statistically noteworthy difference was observed (P > 0.05).]. 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:18849534;
    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:NP58986.RABqjqAcC_qpCbKXYTjmgfJx4_A92uH3AaV0lDkW3FPKk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}