@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP294336.RApY8pmc9nUhmGLOzszMih8H_OVxrG0UDjoJa52NqlKzI> .
@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:NP294336.RApY8pmc9nUhmGLOzszMih8H_OVxrG0UDjoJa52NqlKzI130_head {
  this: np:hasAssertion dgn-np:NP294336.RApY8pmc9nUhmGLOzszMih8H_OVxrG0UDjoJa52NqlKzI130_assertion;
    np:hasProvenance dgn-np:NP294336.RApY8pmc9nUhmGLOzszMih8H_OVxrG0UDjoJa52NqlKzI130_provenance;
    np:hasPublicationInfo dgn-np:NP294336.RApY8pmc9nUhmGLOzszMih8H_OVxrG0UDjoJa52NqlKzI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP294336.RApY8pmc9nUhmGLOzszMih8H_OVxrG0UDjoJa52NqlKzI130_assertion a np:Assertion .
  
  dgn-np:NP294336.RApY8pmc9nUhmGLOzszMih8H_OVxrG0UDjoJa52NqlKzI130_provenance a np:Provenance .
  
  dgn-np:NP294336.RApY8pmc9nUhmGLOzszMih8H_OVxrG0UDjoJa52NqlKzI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP294336.RApY8pmc9nUhmGLOzszMih8H_OVxrG0UDjoJa52NqlKzI130_assertion {
  miriam-gene:6716 a ncit:C16612 .
  
  lld:C0042755 a ncit:C7057 .
  
  dgn-gda:DGN4763af703d7436f463862e41e2bcb44e sio:SIO_000628 miriam-gene:6716, lld:C0042755;
    a sio:SIO_001121 .
}

dgn-np:NP294336.RApY8pmc9nUhmGLOzszMih8H_OVxrG0UDjoJa52NqlKzI130_provenance {
  dgn-np:NP294336.RApY8pmc9nUhmGLOzszMih8H_OVxrG0UDjoJa52NqlKzI130_assertion dcterms:description
      "[A classification based on the severity of the masculinization defect may be used for correlation of phenotypes with enzyme activities and genotypes, and for comparisons of phenotypes between different patients as the basis for clinical decisions to be made in patients with pseudohermaphroditism due to steroid 5 alpha-reductase 2 deficiency.]. 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:8723114;
    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:NP294336.RApY8pmc9nUhmGLOzszMih8H_OVxrG0UDjoJa52NqlKzI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:47+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" .
}