@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP203468.RABc4cFLCcn29dNMjgCmqk6ml2OvR8q-tU4qCT3DKvjS4> .
@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:NP203468.RABc4cFLCcn29dNMjgCmqk6ml2OvR8q-tU4qCT3DKvjS4130_head {
  this: np:hasAssertion dgn-np:NP203468.RABc4cFLCcn29dNMjgCmqk6ml2OvR8q-tU4qCT3DKvjS4130_assertion;
    np:hasProvenance dgn-np:NP203468.RABc4cFLCcn29dNMjgCmqk6ml2OvR8q-tU4qCT3DKvjS4130_provenance;
    np:hasPublicationInfo dgn-np:NP203468.RABc4cFLCcn29dNMjgCmqk6ml2OvR8q-tU4qCT3DKvjS4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP203468.RABc4cFLCcn29dNMjgCmqk6ml2OvR8q-tU4qCT3DKvjS4130_assertion a np:Assertion .
  
  dgn-np:NP203468.RABc4cFLCcn29dNMjgCmqk6ml2OvR8q-tU4qCT3DKvjS4130_provenance a np:Provenance .
  
  dgn-np:NP203468.RABc4cFLCcn29dNMjgCmqk6ml2OvR8q-tU4qCT3DKvjS4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP203468.RABc4cFLCcn29dNMjgCmqk6ml2OvR8q-tU4qCT3DKvjS4130_assertion {
  miriam-gene:551 a ncit:C16612 .
  
  lld:C1809471 a ncit:C7057 .
  
  dgn-gda:DGN66e4b66c984f4feaa15dcd26fa0877cc sio:SIO_000628 miriam-gene:551, lld:C1809471;
    a sio:SIO_001121 .
}

dgn-np:NP203468.RABc4cFLCcn29dNMjgCmqk6ml2OvR8q-tU4qCT3DKvjS4130_provenance {
  dgn-np:NP203468.RABc4cFLCcn29dNMjgCmqk6ml2OvR8q-tU4qCT3DKvjS4130_assertion dcterms:description
      "[We have engineered 11 CaR mutants that have been described in the disorders familial benign hypercalcemia (FBH), neonatal severe hyperparathyroidism (NSHPT), and autosomal dominant hypocalcaemia (ADH), and studied their function by characterizing intracellular calcium [Ca2+]i transients in response to varying concentrations of extracellular calcium [Ca2+]o or gadolinium [Gd3+]o.]. 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:8878438;
    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:NP203468.RABc4cFLCcn29dNMjgCmqk6ml2OvR8q-tU4qCT3DKvjS4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:52+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" .
}