@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP173831.RAZWOPQdcfT5pfm8oSlS8N3LWpFaEUAe0QS_I-xMI-uhA> .
@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:NP173831.RAZWOPQdcfT5pfm8oSlS8N3LWpFaEUAe0QS_I-xMI-uhA130_head {
  this: np:hasAssertion dgn-np:NP173831.RAZWOPQdcfT5pfm8oSlS8N3LWpFaEUAe0QS_I-xMI-uhA130_assertion;
    np:hasProvenance dgn-np:NP173831.RAZWOPQdcfT5pfm8oSlS8N3LWpFaEUAe0QS_I-xMI-uhA130_provenance;
    np:hasPublicationInfo dgn-np:NP173831.RAZWOPQdcfT5pfm8oSlS8N3LWpFaEUAe0QS_I-xMI-uhA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP173831.RAZWOPQdcfT5pfm8oSlS8N3LWpFaEUAe0QS_I-xMI-uhA130_assertion a np:Assertion .
  
  dgn-np:NP173831.RAZWOPQdcfT5pfm8oSlS8N3LWpFaEUAe0QS_I-xMI-uhA130_provenance a np:Provenance .
  
  dgn-np:NP173831.RAZWOPQdcfT5pfm8oSlS8N3LWpFaEUAe0QS_I-xMI-uhA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP173831.RAZWOPQdcfT5pfm8oSlS8N3LWpFaEUAe0QS_I-xMI-uhA130_assertion {
  miriam-gene:1594 a ncit:C16612 .
  
  lld:C0020438 a ncit:C7057 .
  
  dgn-gda:DGN91bbbeb82e3a514bdc0c02baefcaadcc sio:SIO_000628 miriam-gene:1594, lld:C0020438;
    a sio:SIO_001121 .
}

dgn-np:NP173831.RAZWOPQdcfT5pfm8oSlS8N3LWpFaEUAe0QS_I-xMI-uhA130_provenance {
  dgn-np:NP173831.RAZWOPQdcfT5pfm8oSlS8N3LWpFaEUAe0QS_I-xMI-uhA130_assertion dcterms:description
      "[On the basis of these results, we propose that the enhanced intestinal calcium absorption invariably seen in absorptive hypercalciuria and attendant symptoms of this disorder are not attributable to mutations of the VDR and are not linked to a common VDR genotype.]. 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:7559881;
    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:NP173831.RAZWOPQdcfT5pfm8oSlS8N3LWpFaEUAe0QS_I-xMI-uhA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:34+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" .
}