@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g> .
@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:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_head {
  this: np:hasAssertion dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_assertion;
    np:hasProvenance dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_provenance;
    np:hasPublicationInfo dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_assertion a np:Assertion .
  
  dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_provenance a np:Provenance .
  
  dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_assertion {
  miriam-gene:54567 a ncit:C16612 .
  
  lld:C1291601 a ncit:C7057 .
  
  dgn-gda:DGNdc2b850200eb99bd740133853324f1b1 sio:SIO_000628 miriam-gene:54567, lld:C1291601;
    a sio:SIO_001121 .
}

dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_provenance {
  dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_assertion dcterms:description
      "[Nonclassical 3 beta-hydroxysteroid dehydrogenase/delta 5-delta 4-isomerase deficiency (NC3 beta HSDD) has been diagnosed in hyperandrogenic women with an increasing frequency during the last 14 yr. Fifteen menarcheal women with androgen excess syndrome, diagnosed with NC3 beta HSDD previously were restudied, in 12 after discontinuation of glucocorticoid treatment, in 2 patients never treated with glucocorticoids, and in 1 both before and after glucocorticoid therapy.]. 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:7989489;
    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:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:44+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>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}