@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP597830.RA9nio0JFkWw9ZiYrG4my_X23n6AMycVyydtjor8HAAzs> .
@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:NP597830.RA9nio0JFkWw9ZiYrG4my_X23n6AMycVyydtjor8HAAzs130_head {
  this: np:hasAssertion dgn-np:NP597830.RA9nio0JFkWw9ZiYrG4my_X23n6AMycVyydtjor8HAAzs130_assertion ;
    np:hasProvenance dgn-np:NP597830.RA9nio0JFkWw9ZiYrG4my_X23n6AMycVyydtjor8HAAzs130_provenance ;
    np:hasPublicationInfo dgn-np:NP597830.RA9nio0JFkWw9ZiYrG4my_X23n6AMycVyydtjor8HAAzs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP597830.RA9nio0JFkWw9ZiYrG4my_X23n6AMycVyydtjor8HAAzs130_assertion a np:Assertion .
  dgn-np:NP597830.RA9nio0JFkWw9ZiYrG4my_X23n6AMycVyydtjor8HAAzs130_provenance a np:Provenance .
  dgn-np:NP597830.RA9nio0JFkWw9ZiYrG4my_X23n6AMycVyydtjor8HAAzs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP597830.RA9nio0JFkWw9ZiYrG4my_X23n6AMycVyydtjor8HAAzs130_assertion {
  miriam-gene:2908 a ncit:C16612 .
  lld:C0595905 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP597830.RA9nio0JFkWw9ZiYrG4my_X23n6AMycVyydtjor8HAAzs130_provenance {
  dgn-np:NP597830.RA9nio0JFkWw9ZiYrG4my_X23n6AMycVyydtjor8HAAzs130_assertion dcterms:description "[These findings reveal selective abnormalities of GR mRNA expression in the lateral OFC in psychiatric illness, which are more specific and may be less influenced by NR3C1 genotype than those of the dorsolateral prefrontal cortex reported previously.]. 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:22812453 ;
    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:NP597830.RA9nio0JFkWw9ZiYrG4my_X23n6AMycVyydtjor8HAAzs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:59+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 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
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}