@prefix dc: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP808693.RAE0XSQnDVqbhy0CBq1rnqv0Z2oQc6jQUmwoLA_2sMDXA> .
@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 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:NP808693.RAE0XSQnDVqbhy0CBq1rnqv0Z2oQc6jQUmwoLA_2sMDXA130_head {
   this: np:hasAssertion dgn-np:NP808693.RAE0XSQnDVqbhy0CBq1rnqv0Z2oQc6jQUmwoLA_2sMDXA130_assertion ;
    np:hasProvenance dgn-np:NP808693.RAE0XSQnDVqbhy0CBq1rnqv0Z2oQc6jQUmwoLA_2sMDXA130_provenance ;
    np:hasPublicationInfo dgn-np:NP808693.RAE0XSQnDVqbhy0CBq1rnqv0Z2oQc6jQUmwoLA_2sMDXA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP808693.RAE0XSQnDVqbhy0CBq1rnqv0Z2oQc6jQUmwoLA_2sMDXA130_assertion a np:Assertion .
  dgn-np:NP808693.RAE0XSQnDVqbhy0CBq1rnqv0Z2oQc6jQUmwoLA_2sMDXA130_provenance a np:Provenance .
  dgn-np:NP808693.RAE0XSQnDVqbhy0CBq1rnqv0Z2oQc6jQUmwoLA_2sMDXA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP808693.RAE0XSQnDVqbhy0CBq1rnqv0Z2oQc6jQUmwoLA_2sMDXA130_assertion {
   miriam-gene:7490 a ncit:C16612 .
  lld:C0018206 a ncit:C7057 .
  dgn-gda:DGNf7dcc884efb0edaad86ec353c2e2ad34 sio:SIO_000628 miriam-gene:7490 , lld:C0018206 ;
    a sio:SIO_001121 .
}
dgn-np:NP808693.RAE0XSQnDVqbhy0CBq1rnqv0Z2oQc6jQUmwoLA_2sMDXA130_provenance {
   dgn-np:NP808693.RAE0XSQnDVqbhy0CBq1rnqv0Z2oQc6jQUmwoLA_2sMDXA130_assertion dc:description "[The expression of the Wilms' tumor suppressor gene WT1 in granulosa and Sertoli cells prompted us to analyze this gene for mutations in 11 granulosa cell tumors, three Leydig cell tumors, and one Sertoli/Leydig cell tumor.]. 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:8504409 ;
    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:NP808693.RAE0XSQnDVqbhy0CBq1rnqv0Z2oQc6jQUmwoLA_2sMDXA130_publicationInfo {
   this: dc:created "2014-10-02T12:40:16+02:00"^^xsd:dateTime ;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dc:rightsHolder dgn-void:IBIGroup ;
    dc:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}