@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1289153.RAN1XoQ_gskGPc8P6XqO0PDMwJlj857keYo3L6RrA0_7k> .
@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:NP1289153.RAN1XoQ_gskGPc8P6XqO0PDMwJlj857keYo3L6RrA0_7k130_head {
  this: np:hasAssertion dgn-np:NP1289153.RAN1XoQ_gskGPc8P6XqO0PDMwJlj857keYo3L6RrA0_7k130_assertion;
    np:hasProvenance dgn-np:NP1289153.RAN1XoQ_gskGPc8P6XqO0PDMwJlj857keYo3L6RrA0_7k130_provenance;
    np:hasPublicationInfo dgn-np:NP1289153.RAN1XoQ_gskGPc8P6XqO0PDMwJlj857keYo3L6RrA0_7k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1289153.RAN1XoQ_gskGPc8P6XqO0PDMwJlj857keYo3L6RrA0_7k130_assertion a np:Assertion .
  
  dgn-np:NP1289153.RAN1XoQ_gskGPc8P6XqO0PDMwJlj857keYo3L6RrA0_7k130_provenance a np:Provenance .
  
  dgn-np:NP1289153.RAN1XoQ_gskGPc8P6XqO0PDMwJlj857keYo3L6RrA0_7k130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1289153.RAN1XoQ_gskGPc8P6XqO0PDMwJlj857keYo3L6RrA0_7k130_assertion {
  miriam-gene:5567 a ncit:C16612 .
  
  lld:C0010481 a ncit:C7057 .
  
  dgn-gda:DGN535ea6c4d85ad4ab5c0cd8408ff847be sio:SIO_000628 miriam-gene:5567, lld:C0010481;
    a sio:SIO_001121 .
}

dgn-np:NP1289153.RAN1XoQ_gskGPc8P6XqO0PDMwJlj857keYo3L6RrA0_7k130_provenance {
  dgn-np:NP1289153.RAN1XoQ_gskGPc8P6XqO0PDMwJlj857keYo3L6RrA0_7k130_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:NP1289153.RAN1XoQ_gskGPc8P6XqO0PDMwJlj857keYo3L6RrA0_7k130_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" .
}