@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU> .
@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:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_head {
  this: np:hasAssertion dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_assertion;
    np:hasProvenance dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_provenance;
    np:hasPublicationInfo dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_assertion a np:Assertion .
  
  dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_provenance a np:Provenance .
  
  dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0001622 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_provenance {
  dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_assertion dcterms:description
      "[The data showed lack of association between BMD and these widely studied VDR polymorphisms, suggesting that the effect of endogenous hypercortisolism on bone in the context of CD does not depend on VDR genotypes.]. 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:22570981;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:57+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}