@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg> .
@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:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_head {
  this: np:hasAssertion dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_assertion;
    np:hasProvenance dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_provenance;
    np:hasPublicationInfo dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_assertion a np:Assertion .
  
  dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_provenance a np:Provenance .
  
  dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_assertion {
  miriam-gene:6736 a ncit:C16612 .
  
  lld:C0042755 a ncit:C7057 .
  
  dgn-gda:DGN3c13186251573ac33016743fa9b11f09 sio:SIO_000628 miriam-gene:6736, lld:C0042755;
    a sio:SIO_001121 .
}

dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_provenance {
  dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_assertion dcterms:description
      "[In this study, five very rare cases of SRY carrying subjects (two XX males and three XX true hermaphrodites) with various degrees of incomplete masculinisation were analysed in order to elucidate the cause of sexual ambiguity despite the presence of the SRY gene.]. 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:10874632;
    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:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:46+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" .
}