@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP266325.RAA6jJNEWVUM5KGEI_Tjl53wkU1WkNzHXQXS9xShCPWaM> .
@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:NP266325.RAA6jJNEWVUM5KGEI_Tjl53wkU1WkNzHXQXS9xShCPWaM130_head {
  this: np:hasAssertion dgn-np:NP266325.RAA6jJNEWVUM5KGEI_Tjl53wkU1WkNzHXQXS9xShCPWaM130_assertion;
    np:hasProvenance dgn-np:NP266325.RAA6jJNEWVUM5KGEI_Tjl53wkU1WkNzHXQXS9xShCPWaM130_provenance;
    np:hasPublicationInfo dgn-np:NP266325.RAA6jJNEWVUM5KGEI_Tjl53wkU1WkNzHXQXS9xShCPWaM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266325.RAA6jJNEWVUM5KGEI_Tjl53wkU1WkNzHXQXS9xShCPWaM130_assertion a np:Assertion .
  
  dgn-np:NP266325.RAA6jJNEWVUM5KGEI_Tjl53wkU1WkNzHXQXS9xShCPWaM130_provenance a np:Provenance .
  
  dgn-np:NP266325.RAA6jJNEWVUM5KGEI_Tjl53wkU1WkNzHXQXS9xShCPWaM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266325.RAA6jJNEWVUM5KGEI_Tjl53wkU1WkNzHXQXS9xShCPWaM130_assertion {
  miriam-gene:846 a ncit:C16612 .
  
  lld:C0262587 a ncit:C7057 .
  
  dgn-gda:DGN68812c0438277e5699f0b31be59888f5 sio:SIO_000628 miriam-gene:846, lld:C0262587;
    a sio:SIO_001121 .
}

dgn-np:NP266325.RAA6jJNEWVUM5KGEI_Tjl53wkU1WkNzHXQXS9xShCPWaM130_provenance {
  dgn-np:NP266325.RAA6jJNEWVUM5KGEI_Tjl53wkU1WkNzHXQXS9xShCPWaM130_assertion dcterms:description
      "[Because reduced expression of CaSR may result in insufficient suppression of parathyroid hormone secretion, the elucidation of regulatory mechanisms of CaSR expression is indispensable for understanding the pathogenesis of parathyroid adenomas.]. 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:10713061;
    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:NP266325.RAA6jJNEWVUM5KGEI_Tjl53wkU1WkNzHXQXS9xShCPWaM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}