@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP887704.RABC0DaEQTJuOUjG-yp3vNsxb94LH7MNeZQ244AMcv0GA> .
@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:NP887704.RABC0DaEQTJuOUjG-yp3vNsxb94LH7MNeZQ244AMcv0GA130_head {
  this: np:hasAssertion dgn-np:NP887704.RABC0DaEQTJuOUjG-yp3vNsxb94LH7MNeZQ244AMcv0GA130_assertion;
    np:hasProvenance dgn-np:NP887704.RABC0DaEQTJuOUjG-yp3vNsxb94LH7MNeZQ244AMcv0GA130_provenance;
    np:hasPublicationInfo dgn-np:NP887704.RABC0DaEQTJuOUjG-yp3vNsxb94LH7MNeZQ244AMcv0GA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP887704.RABC0DaEQTJuOUjG-yp3vNsxb94LH7MNeZQ244AMcv0GA130_assertion a np:Assertion .
  
  dgn-np:NP887704.RABC0DaEQTJuOUjG-yp3vNsxb94LH7MNeZQ244AMcv0GA130_provenance a np:Provenance .
  
  dgn-np:NP887704.RABC0DaEQTJuOUjG-yp3vNsxb94LH7MNeZQ244AMcv0GA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP887704.RABC0DaEQTJuOUjG-yp3vNsxb94LH7MNeZQ244AMcv0GA130_assertion {
  miriam-gene:1594 a ncit:C16612 .
  
  lld:C0020502 a ncit:C7057 .
  
  dgn-gda:DGNfb8c177762566a1b1690d06751b600ac sio:SIO_000628 miriam-gene:1594, lld:C0020502;
    a sio:SIO_001121 .
}

dgn-np:NP887704.RABC0DaEQTJuOUjG-yp3vNsxb94LH7MNeZQ244AMcv0GA130_provenance {
  dgn-np:NP887704.RABC0DaEQTJuOUjG-yp3vNsxb94LH7MNeZQ244AMcv0GA130_assertion dcterms:description
      "[Using conventional riboprobe in situ hybridization, VDR transcripts were readily detectable in osteoblasts within sections taken from normal bone and several actively remodelling bone tissues, namely, Paget's disease, renal hyperparathyroidism, and healing fracture callus.]. 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:8726384;
    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:NP887704.RABC0DaEQTJuOUjG-yp3vNsxb94LH7MNeZQ244AMcv0GA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:05+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" .
}