@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP798629.RATeEeHQS5nFpxTLaCCFZ0ZCobImeUladBtu143R3WDRk> .
@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:NP798629.RATeEeHQS5nFpxTLaCCFZ0ZCobImeUladBtu143R3WDRk130_head {
  this: np:hasAssertion dgn-np:NP798629.RATeEeHQS5nFpxTLaCCFZ0ZCobImeUladBtu143R3WDRk130_assertion ;
    np:hasProvenance dgn-np:NP798629.RATeEeHQS5nFpxTLaCCFZ0ZCobImeUladBtu143R3WDRk130_provenance ;
    np:hasPublicationInfo dgn-np:NP798629.RATeEeHQS5nFpxTLaCCFZ0ZCobImeUladBtu143R3WDRk130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP798629.RATeEeHQS5nFpxTLaCCFZ0ZCobImeUladBtu143R3WDRk130_provenance a np:Provenance .
  dgn-np:NP798629.RATeEeHQS5nFpxTLaCCFZ0ZCobImeUladBtu143R3WDRk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP798629.RATeEeHQS5nFpxTLaCCFZ0ZCobImeUladBtu143R3WDRk130_assertion {
  miriam-gene:1586 a ncit:C16612 .
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    a sio:SIO_001121 .
}
dgn-np:NP798629.RATeEeHQS5nFpxTLaCCFZ0ZCobImeUladBtu143R3WDRk130_provenance {
  dgn-np:NP798629.RATeEeHQS5nFpxTLaCCFZ0ZCobImeUladBtu143R3WDRk130_assertion dcterms:description "[The aim of this study was to compare clinical data with mRNA expression of CYP17 and CYP11B1 in adrenocortical tumors from patients with and without Cushing's syndrome and to identify adrenal tumors that may cause subclinical 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 ;
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    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:NP798629.RATeEeHQS5nFpxTLaCCFZ0ZCobImeUladBtu143R3WDRk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:10+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}