@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP781694.RARX3CctuhMvlhHOPU4U4vleB0gRuM7j5aECQb5-GfGoY> .
@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:NP781694.RARX3CctuhMvlhHOPU4U4vleB0gRuM7j5aECQb5-GfGoY130_head {
  this: np:hasAssertion dgn-np:NP781694.RARX3CctuhMvlhHOPU4U4vleB0gRuM7j5aECQb5-GfGoY130_assertion;
    np:hasProvenance dgn-np:NP781694.RARX3CctuhMvlhHOPU4U4vleB0gRuM7j5aECQb5-GfGoY130_provenance;
    np:hasPublicationInfo dgn-np:NP781694.RARX3CctuhMvlhHOPU4U4vleB0gRuM7j5aECQb5-GfGoY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP781694.RARX3CctuhMvlhHOPU4U4vleB0gRuM7j5aECQb5-GfGoY130_assertion a np:Assertion .
  
  dgn-np:NP781694.RARX3CctuhMvlhHOPU4U4vleB0gRuM7j5aECQb5-GfGoY130_provenance a np:Provenance .
  
  dgn-np:NP781694.RARX3CctuhMvlhHOPU4U4vleB0gRuM7j5aECQb5-GfGoY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP781694.RARX3CctuhMvlhHOPU4U4vleB0gRuM7j5aECQb5-GfGoY130_assertion {
  miriam-gene:5741 a ncit:C16612 .
  
  lld:C0031511 a ncit:C7057 .
  
  dgn-gda:DGN68aa8e16461ac354a78b6757d14d04bc sio:SIO_000628 miriam-gene:5741, lld:C0031511;
    a sio:SIO_001121 .
}

dgn-np:NP781694.RARX3CctuhMvlhHOPU4U4vleB0gRuM7j5aECQb5-GfGoY130_provenance {
  dgn-np:NP781694.RARX3CctuhMvlhHOPU4U4vleB0gRuM7j5aECQb5-GfGoY130_assertion dcterms:description
      "[Although PPHP does not have the biochemical features of hypocalcemia and elevated parathyroid hormone levels as seen in pseudohypoparathyroidism, it seems from this case to share the potential for multiple endocrine neoplasia seen in a number of metabolic disorders in which pheochromocytoma may be a prominent manifestation.]. 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:6870447;
    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:NP781694.RARX3CctuhMvlhHOPU4U4vleB0gRuM7j5aECQb5-GfGoY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:53+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" .
}