@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP841714.RA0cL6Hk0ydCLIBYT3VIRQaMNH0IIhnflJnZU3Y-cXOfc> .
@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:NP841714.RA0cL6Hk0ydCLIBYT3VIRQaMNH0IIhnflJnZU3Y-cXOfc130_head {
  this: np:hasAssertion dgn-np:NP841714.RA0cL6Hk0ydCLIBYT3VIRQaMNH0IIhnflJnZU3Y-cXOfc130_assertion;
    np:hasProvenance dgn-np:NP841714.RA0cL6Hk0ydCLIBYT3VIRQaMNH0IIhnflJnZU3Y-cXOfc130_provenance;
    np:hasPublicationInfo dgn-np:NP841714.RA0cL6Hk0ydCLIBYT3VIRQaMNH0IIhnflJnZU3Y-cXOfc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP841714.RA0cL6Hk0ydCLIBYT3VIRQaMNH0IIhnflJnZU3Y-cXOfc130_assertion a np:Assertion .
  
  dgn-np:NP841714.RA0cL6Hk0ydCLIBYT3VIRQaMNH0IIhnflJnZU3Y-cXOfc130_provenance a np:Provenance .
  
  dgn-np:NP841714.RA0cL6Hk0ydCLIBYT3VIRQaMNH0IIhnflJnZU3Y-cXOfc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP841714.RA0cL6Hk0ydCLIBYT3VIRQaMNH0IIhnflJnZU3Y-cXOfc130_assertion {
  miriam-gene:2908 a ncit:C16612 .
  
  lld:C0234235 a ncit:C7057 .
  
  dgn-gda:DGNbee2447232d18c3f5ed2fa6d6e378630 sio:SIO_000628 miriam-gene:2908, lld:C0234235;
    a sio:SIO_001121 .
}

dgn-np:NP841714.RA0cL6Hk0ydCLIBYT3VIRQaMNH0IIhnflJnZU3Y-cXOfc130_provenance {
  dgn-np:NP841714.RA0cL6Hk0ydCLIBYT3VIRQaMNH0IIhnflJnZU3Y-cXOfc130_assertion dcterms:description
      "[The molecular basis of Chrousos syndrome and PGGH has been ascribed to mutations in the gene encoding the human glucocorticoid receptor (hGR), which impair glucocorticoid signal transduction and alter tissue sensitivity to glucocorticoids.]. 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:23033539;
    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:NP841714.RA0cL6Hk0ydCLIBYT3VIRQaMNH0IIhnflJnZU3Y-cXOfc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:34+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" .
}