@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP819843.RAUCbypewCmPTpfLhhUPg1HSSp9tpLoJObyXWiNFAEJMo> .
@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:NP819843.RAUCbypewCmPTpfLhhUPg1HSSp9tpLoJObyXWiNFAEJMo130_head {
  this: np:hasAssertion dgn-np:NP819843.RAUCbypewCmPTpfLhhUPg1HSSp9tpLoJObyXWiNFAEJMo130_assertion;
    np:hasProvenance dgn-np:NP819843.RAUCbypewCmPTpfLhhUPg1HSSp9tpLoJObyXWiNFAEJMo130_provenance;
    np:hasPublicationInfo dgn-np:NP819843.RAUCbypewCmPTpfLhhUPg1HSSp9tpLoJObyXWiNFAEJMo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP819843.RAUCbypewCmPTpfLhhUPg1HSSp9tpLoJObyXWiNFAEJMo130_assertion a np:Assertion .
  
  dgn-np:NP819843.RAUCbypewCmPTpfLhhUPg1HSSp9tpLoJObyXWiNFAEJMo130_provenance a np:Provenance .
  
  dgn-np:NP819843.RAUCbypewCmPTpfLhhUPg1HSSp9tpLoJObyXWiNFAEJMo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP819843.RAUCbypewCmPTpfLhhUPg1HSSp9tpLoJObyXWiNFAEJMo130_assertion {
  miriam-gene:846 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP819843.RAUCbypewCmPTpfLhhUPg1HSSp9tpLoJObyXWiNFAEJMo130_provenance {
  dgn-np:NP819843.RAUCbypewCmPTpfLhhUPg1HSSp9tpLoJObyXWiNFAEJMo130_assertion dcterms:description
      "[This review covers current knowledge of the role of the CaSR in disorders of calcium homeostasis (FHH, neonatal severe hyperparathyroidism, autosomal dominant hypocalcemia, primary and secondary hyperparathyroidism, hypercalcemia of malignancy) as well as unrelated diseases such as breast and colorectal cancer (where the receptor appears to play a tumor suppressor role), Alzheimer's disease, pancreatitis, diabetes mellitus, hypertension and bone and gastrointestinal disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP819843.RAUCbypewCmPTpfLhhUPg1HSSp9tpLoJObyXWiNFAEJMo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:22+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;
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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" .
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