@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1289152.RApFsu0LKOScLiX9boqCUfsf1APo57VTRsXovWqs7goqk> .
@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:NP1289152.RApFsu0LKOScLiX9boqCUfsf1APo57VTRsXovWqs7goqk130_head {
  this: np:hasAssertion dgn-np:NP1289152.RApFsu0LKOScLiX9boqCUfsf1APo57VTRsXovWqs7goqk130_assertion;
    np:hasProvenance dgn-np:NP1289152.RApFsu0LKOScLiX9boqCUfsf1APo57VTRsXovWqs7goqk130_provenance;
    np:hasPublicationInfo dgn-np:NP1289152.RApFsu0LKOScLiX9boqCUfsf1APo57VTRsXovWqs7goqk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1289152.RApFsu0LKOScLiX9boqCUfsf1APo57VTRsXovWqs7goqk130_assertion a np:Assertion .
  
  dgn-np:NP1289152.RApFsu0LKOScLiX9boqCUfsf1APo57VTRsXovWqs7goqk130_provenance a np:Provenance .
  
  dgn-np:NP1289152.RApFsu0LKOScLiX9boqCUfsf1APo57VTRsXovWqs7goqk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1289152.RApFsu0LKOScLiX9boqCUfsf1APo57VTRsXovWqs7goqk130_assertion {
  miriam-gene:5573 a ncit:C16612 .
  
  lld:C0010481 a ncit:C7057 .
  
  dgn-gda:DGN7244a3c41c5d30e2f6a2da4c252e1453 sio:SIO_000628 miriam-gene:5573, lld:C0010481;
    a sio:SIO_001121 .
}

dgn-np:NP1289152.RApFsu0LKOScLiX9boqCUfsf1APo57VTRsXovWqs7goqk130_provenance {
  dgn-np:NP1289152.RApFsu0LKOScLiX9boqCUfsf1APo57VTRsXovWqs7goqk130_assertion dcterms:description
      "[In this report, we review CNC, its clinical features, diagnosis, treatment and molecular etiology, including PRKAR1A mutations and the newest on PRKACA and PRKACB defects especially as they pertain to adrenal tumors and Cushing's syndrome.]. 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:26130139;
    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:NP1289152.RApFsu0LKOScLiX9boqCUfsf1APo57VTRsXovWqs7goqk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:30+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" .
}