@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP533828.RADZE-eLBJdYmG0dj2a1cJBQWnOLqV73Roq3loMZrAV40> .
@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:NP533828.RADZE-eLBJdYmG0dj2a1cJBQWnOLqV73Roq3loMZrAV40130_head {
  this: np:hasAssertion dgn-np:NP533828.RADZE-eLBJdYmG0dj2a1cJBQWnOLqV73Roq3loMZrAV40130_assertion ;
    np:hasProvenance dgn-np:NP533828.RADZE-eLBJdYmG0dj2a1cJBQWnOLqV73Roq3loMZrAV40130_provenance ;
    np:hasPublicationInfo dgn-np:NP533828.RADZE-eLBJdYmG0dj2a1cJBQWnOLqV73Roq3loMZrAV40130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP533828.RADZE-eLBJdYmG0dj2a1cJBQWnOLqV73Roq3loMZrAV40130_provenance a np:Provenance .
  dgn-np:NP533828.RADZE-eLBJdYmG0dj2a1cJBQWnOLqV73Roq3loMZrAV40130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP533828.RADZE-eLBJdYmG0dj2a1cJBQWnOLqV73Roq3loMZrAV40130_assertion {
  miriam-gene:5573 a ncit:C16612 .
  lld:C1857451 a ncit:C7057 .
  dgn-gda:DGNec83339f0a88a041a7439e989b67c257 sio:SIO_000628 miriam-gene:5573 , lld:C1857451 ;
    a sio:SIO_001121 .
}
dgn-np:NP533828.RADZE-eLBJdYmG0dj2a1cJBQWnOLqV73Roq3loMZrAV40130_provenance {
  dgn-np:NP533828.RADZE-eLBJdYmG0dj2a1cJBQWnOLqV73Roq3loMZrAV40130_assertion dcterms:description "[Cortisol-producing hyperplasia of the adrenal glands is caused by two distinct syndromes, both of which have been directly or indirectly associated with protein kinase A signaling: (i) primary pigmented nodular adrenocortical disease (PPNAD) (a micronodular form of bilateral adrenal hyperplasia), either isolated (rarely) or in the context of Carney complex, is caused (in most cases) by mutations of the PRKAR1A gene; and (ii) ACTH-independent macronodular adrenal hyperplasia (AIMAH), or massive macronodular adrenal disease (MMAD), has been associated with aberrant (ectopic) expression, and presumably regulation, of various G protein-coupled receptors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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:NP533828.RADZE-eLBJdYmG0dj2a1cJBQWnOLqV73Roq3loMZrAV40130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:22+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> ;
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}