@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP203294.RASjXQ7AII3xGwxbSULKVBp9i9nin-EUrZLDDYUw9qkGk> .
@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:NP203294.RASjXQ7AII3xGwxbSULKVBp9i9nin-EUrZLDDYUw9qkGk130_head {
  this: np:hasAssertion dgn-np:NP203294.RASjXQ7AII3xGwxbSULKVBp9i9nin-EUrZLDDYUw9qkGk130_assertion;
    np:hasProvenance dgn-np:NP203294.RASjXQ7AII3xGwxbSULKVBp9i9nin-EUrZLDDYUw9qkGk130_provenance;
    np:hasPublicationInfo dgn-np:NP203294.RASjXQ7AII3xGwxbSULKVBp9i9nin-EUrZLDDYUw9qkGk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP203294.RASjXQ7AII3xGwxbSULKVBp9i9nin-EUrZLDDYUw9qkGk130_assertion a np:Assertion .
  
  dgn-np:NP203294.RASjXQ7AII3xGwxbSULKVBp9i9nin-EUrZLDDYUw9qkGk130_provenance a np:Provenance .
  
  dgn-np:NP203294.RASjXQ7AII3xGwxbSULKVBp9i9nin-EUrZLDDYUw9qkGk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP203294.RASjXQ7AII3xGwxbSULKVBp9i9nin-EUrZLDDYUw9qkGk130_assertion {
  miriam-gene:1589 a ncit:C16612 .
  
  lld:C0342546 a ncit:C7057 .
  
  dgn-gda:DGNbc523d8da8f35ac34cb7ab4f828425a4 sio:SIO_000628 miriam-gene:1589, lld:C0342546;
    a sio:SIO_001121 .
}

dgn-np:NP203294.RASjXQ7AII3xGwxbSULKVBp9i9nin-EUrZLDDYUw9qkGk130_provenance {
  dgn-np:NP203294.RASjXQ7AII3xGwxbSULKVBp9i9nin-EUrZLDDYUw9qkGk130_assertion dcterms:description
      "[To determine the role of 21-hydroxylase (CYP21) gene mutations in these disorders, we performed molecular genotype analysis on 48 children and adolescents referred for evaluation of hyperandrogenic findings and diagnosed as having premature adrenarche or functional androgen excess.]. 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:9441866;
    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:NP203294.RASjXQ7AII3xGwxbSULKVBp9i9nin-EUrZLDDYUw9qkGk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:52+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>,
      <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" .
}