@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs> .
@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:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_head {
  this: np:hasAssertion dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_assertion;
    np:hasProvenance dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_provenance;
    np:hasPublicationInfo dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_assertion a np:Assertion .
  
  dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_provenance a np:Provenance .
  
  dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0520463 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_provenance {
  dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_assertion dcterms:description
      "[This study assessed the clinical and laboratory factors involved in BMD of 45 patients at the Pediatric Unit of Endocrinology, UNICAMP, who had been diagnosed as having classical CAH due to CYP21A2 deficiency including molecular characterization.]. 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:14586796;
    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:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:52+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}