@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP580964.RAaTAjzU2FtAq0D5Vv8PjPq8TDeF52eYidcT-15rx25_o> .
@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:NP580964.RAaTAjzU2FtAq0D5Vv8PjPq8TDeF52eYidcT-15rx25_o130_head {
  this: np:hasAssertion dgn-np:NP580964.RAaTAjzU2FtAq0D5Vv8PjPq8TDeF52eYidcT-15rx25_o130_assertion;
    np:hasProvenance dgn-np:NP580964.RAaTAjzU2FtAq0D5Vv8PjPq8TDeF52eYidcT-15rx25_o130_provenance;
    np:hasPublicationInfo dgn-np:NP580964.RAaTAjzU2FtAq0D5Vv8PjPq8TDeF52eYidcT-15rx25_o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP580964.RAaTAjzU2FtAq0D5Vv8PjPq8TDeF52eYidcT-15rx25_o130_assertion a np:Assertion .
  
  dgn-np:NP580964.RAaTAjzU2FtAq0D5Vv8PjPq8TDeF52eYidcT-15rx25_o130_provenance a np:Provenance .
  
  dgn-np:NP580964.RAaTAjzU2FtAq0D5Vv8PjPq8TDeF52eYidcT-15rx25_o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP580964.RAaTAjzU2FtAq0D5Vv8PjPq8TDeF52eYidcT-15rx25_o130_assertion {
  miriam-gene:1594 a ncit:C16612 .
  
  lld:C1336076 a ncit:C7057 .
  
  dgn-gda:DGNe8d7611b281b31f7495158a759f62650 sio:SIO_000628 miriam-gene:1594, lld:C1336076;
    a sio:SIO_001121 .
}

dgn-np:NP580964.RAaTAjzU2FtAq0D5Vv8PjPq8TDeF52eYidcT-15rx25_o130_provenance {
  dgn-np:NP580964.RAaTAjzU2FtAq0D5Vv8PjPq8TDeF52eYidcT-15rx25_o130_assertion dcterms:description
      "[These results suggest that polymorphic variation in or near the 3' end of the VDR gene may influence breast cancer risk in Taiwanese women and justifies further investigation of the role of VDR for sporadic breast cancer in low-incidence areas.]. 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:12150447;
    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:NP580964.RAaTAjzU2FtAq0D5Vv8PjPq8TDeF52eYidcT-15rx25_o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:50+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" .
}