@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_head {
  this: np:hasAssertion dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_assertion ;
    np:hasProvenance dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_provenance ;
    np:hasPublicationInfo dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_assertion a np:Assertion .
  dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_provenance a np:Provenance .
  dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_assertion {
  miriam-gene:138428 a ncit:C16612 .
  lld:C0020437 a ncit:C7057 .
  dgn-gda:DGNea8549c822ea2342c4f192a11288791a sio:SIO_000628 miriam-gene:138428 , lld:C0020437 ;
    a sio:SIO_001121 .
}
dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_provenance {
  dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_assertion dcterms:description "[In a case of neonatal severe hyperparathyroidism characterized by moderately severe hypercalcemia and very high PTH levels, coupled with evidence of hyperparathyroidism and effects on brain development not previously demonstrated, we detected point mutations on separate alleles of the CaR, resulting in premature stop codon substitutions at G94 and R648.]. 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:15292296 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:11+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}