@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP376896.RAcLxE5HmufHvzBtcjMfCiTUZpAmAvhR6ExVXv9NyMuhI> .
@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:NP376896.RAcLxE5HmufHvzBtcjMfCiTUZpAmAvhR6ExVXv9NyMuhI130_head {
  this: np:hasAssertion dgn-np:NP376896.RAcLxE5HmufHvzBtcjMfCiTUZpAmAvhR6ExVXv9NyMuhI130_assertion;
    np:hasProvenance dgn-np:NP376896.RAcLxE5HmufHvzBtcjMfCiTUZpAmAvhR6ExVXv9NyMuhI130_provenance;
    np:hasPublicationInfo dgn-np:NP376896.RAcLxE5HmufHvzBtcjMfCiTUZpAmAvhR6ExVXv9NyMuhI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP376896.RAcLxE5HmufHvzBtcjMfCiTUZpAmAvhR6ExVXv9NyMuhI130_assertion a np:Assertion .
  
  dgn-np:NP376896.RAcLxE5HmufHvzBtcjMfCiTUZpAmAvhR6ExVXv9NyMuhI130_provenance a np:Provenance .
  
  dgn-np:NP376896.RAcLxE5HmufHvzBtcjMfCiTUZpAmAvhR6ExVXv9NyMuhI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP376896.RAcLxE5HmufHvzBtcjMfCiTUZpAmAvhR6ExVXv9NyMuhI130_assertion {
  miriam-gene:8170 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN07a710e0feea612bdfbb43df2380fa59 sio:SIO_000628 miriam-gene:8170, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP376896.RAcLxE5HmufHvzBtcjMfCiTUZpAmAvhR6ExVXv9NyMuhI130_provenance {
  dgn-np:NP376896.RAcLxE5HmufHvzBtcjMfCiTUZpAmAvhR6ExVXv9NyMuhI130_assertion dcterms:description
      "[Five polymorphic variants of the VDR gene, including Cdx-2 (intron 1e) and FokI (exon 2) present in the 5' region of the gene, and BsmI (intron 8), ApaI (intron 8), and TaqI (exon 9) sites present in the 3' untranslated region (UTR), were evaluated for possible associations with colorectal cancer risk.]. 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:22529698;
    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:NP376896.RAcLxE5HmufHvzBtcjMfCiTUZpAmAvhR6ExVXv9NyMuhI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:40+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" .
}