@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1284752.RA9wVIFLdebPn0WAg05kn9Qofr984yzQu32knMqZYFvHk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1284752.RA9wVIFLdebPn0WAg05kn9Qofr984yzQu32knMqZYFvHk130_head {
  this: np:hasAssertion dgn-np:NP1284752.RA9wVIFLdebPn0WAg05kn9Qofr984yzQu32knMqZYFvHk130_assertion;
    np:hasProvenance dgn-np:NP1284752.RA9wVIFLdebPn0WAg05kn9Qofr984yzQu32knMqZYFvHk130_provenance;
    np:hasPublicationInfo dgn-np:NP1284752.RA9wVIFLdebPn0WAg05kn9Qofr984yzQu32knMqZYFvHk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1284752.RA9wVIFLdebPn0WAg05kn9Qofr984yzQu32knMqZYFvHk130_assertion a np:Assertion .
  
  dgn-np:NP1284752.RA9wVIFLdebPn0WAg05kn9Qofr984yzQu32knMqZYFvHk130_provenance a np:Provenance .
  
  dgn-np:NP1284752.RA9wVIFLdebPn0WAg05kn9Qofr984yzQu32knMqZYFvHk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1284752.RA9wVIFLdebPn0WAg05kn9Qofr984yzQu32knMqZYFvHk130_assertion {
  miriam-gene:2516 a ncit:C16612 .
  
  lld:C0001403 a ncit:C7057 .
  
  dgn-gda:DGN219e41f1e72d7cfa3eac5b52cff7087d sio:SIO_000628 miriam-gene:2516, lld:C0001403;
    a sio:SIO_001121 .
}

dgn-np:NP1284752.RA9wVIFLdebPn0WAg05kn9Qofr984yzQu32knMqZYFvHk130_provenance {
  dgn-np:NP1284752.RA9wVIFLdebPn0WAg05kn9Qofr984yzQu32knMqZYFvHk130_assertion dcterms:description
      "[Mutations in NR5A1 have been initially associated with primary adrenal insufficiency and 46,XY gonadal dysgenesis and more recently with less severe phenotypes, including preliminary descriptions in severe forms of male factor infertility.]. 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:25989977;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1284752.RA9wVIFLdebPn0WAg05kn9Qofr984yzQu32knMqZYFvHk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:28+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}