@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM> .
@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:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_head {
  this: np:hasAssertion dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_assertion;
    np:hasProvenance dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_provenance;
    np:hasPublicationInfo dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_assertion a np:Assertion .
  
  dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_provenance a np:Provenance .
  
  dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_assertion {
  miriam-gene:7421 a ncit:C16612 .
  
  lld:C0033578 a ncit:C7057 .
  
  dgn-gda:DGN4d50e1a250f4fe38ed419cea5c83bc32 sio:SIO_000628 miriam-gene:7421, lld:C0033578;
    a sio:SIO_001122 .
}

dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_provenance {
  dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_assertion dcterms:description
      "[no correlation of VDR gene polymorphisms, as detected by Apal and Taql restriction fragments, in multiethnic Brazilian men (165 patients and 200 controls) with prostate cancer risk and parameters of disease severity was found ]. 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:15503828;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:53+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" .
}