@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP484370.RAaCdm2aA7F2pnky6alcGeeaYlmMjlntvMYwkyyk4d6Jw> .
@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:NP484370.RAaCdm2aA7F2pnky6alcGeeaYlmMjlntvMYwkyyk4d6Jw130_head {
  this: np:hasAssertion dgn-np:NP484370.RAaCdm2aA7F2pnky6alcGeeaYlmMjlntvMYwkyyk4d6Jw130_assertion;
    np:hasProvenance dgn-np:NP484370.RAaCdm2aA7F2pnky6alcGeeaYlmMjlntvMYwkyyk4d6Jw130_provenance;
    np:hasPublicationInfo dgn-np:NP484370.RAaCdm2aA7F2pnky6alcGeeaYlmMjlntvMYwkyyk4d6Jw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP484370.RAaCdm2aA7F2pnky6alcGeeaYlmMjlntvMYwkyyk4d6Jw130_assertion a np:Assertion .
  
  dgn-np:NP484370.RAaCdm2aA7F2pnky6alcGeeaYlmMjlntvMYwkyyk4d6Jw130_provenance a np:Provenance .
  
  dgn-np:NP484370.RAaCdm2aA7F2pnky6alcGeeaYlmMjlntvMYwkyyk4d6Jw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP484370.RAaCdm2aA7F2pnky6alcGeeaYlmMjlntvMYwkyyk4d6Jw130_assertion {
  miriam-gene:846 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
  dgn-gda:DGNce75de18c85aab293aed28a69ddf23b8 sio:SIO_000628 miriam-gene:846, lld:C0596263;
    a sio:SIO_001121 .
}

dgn-np:NP484370.RAaCdm2aA7F2pnky6alcGeeaYlmMjlntvMYwkyyk4d6Jw130_provenance {
  dgn-np:NP484370.RAaCdm2aA7F2pnky6alcGeeaYlmMjlntvMYwkyyk4d6Jw130_assertion dcterms:description
      "[Although mutation of the CaR does not appear to be an early event in carcinogenesis, loss or upregulation of normal CaR function can contribute to several aspects of neoplastic progression, so that therapeutic strategies directed at the CaR could potentially serve a supportive function in cancer management.]. 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:15200153;
    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:NP484370.RAaCdm2aA7F2pnky6alcGeeaYlmMjlntvMYwkyyk4d6Jw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:49+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" .
}