@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs> .
@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:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_head {
  this: np:hasAssertion dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_assertion ;
    np:hasProvenance dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_provenance ;
    np:hasPublicationInfo dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_assertion a np:Assertion .
  dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_provenance a np:Provenance .
  dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_assertion {
  miriam-gene:138428 a ncit:C16612 .
  lld:C0342637 a ncit:C7057 .
  dgn-gda:DGNd8f60a3db2c76fec45169e4ba02dcb0e sio:SIO_000628 miriam-gene:138428 , lld:C0342637 ;
    a sio:SIO_001121 .
}
dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_provenance {
  dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_assertion dcterms:description "[Therefore, a biochemical phenotype of PTH-dependent hypercalcemia resembling that caused by heterozygous inactivating mutations of the CaR in familial hypocalciuric hypercalcemia can be observed in patients with antibodies to the CaR's extracellular domain that stimulate PTH release, probably by inhibiting activation of the CaR by Ca(2+)(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:12519831 ;
    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:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:20+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" .
}