@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP219956.RAxE11goTjDR0qYREs4sa4ps7kli_aNunR3OEX99GFB24> .
@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:NP219956.RAxE11goTjDR0qYREs4sa4ps7kli_aNunR3OEX99GFB24130_head {
  this: np:hasAssertion dgn-np:NP219956.RAxE11goTjDR0qYREs4sa4ps7kli_aNunR3OEX99GFB24130_assertion ;
    np:hasProvenance dgn-np:NP219956.RAxE11goTjDR0qYREs4sa4ps7kli_aNunR3OEX99GFB24130_provenance ;
    np:hasPublicationInfo dgn-np:NP219956.RAxE11goTjDR0qYREs4sa4ps7kli_aNunR3OEX99GFB24130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP219956.RAxE11goTjDR0qYREs4sa4ps7kli_aNunR3OEX99GFB24130_assertion a np:Assertion .
  dgn-np:NP219956.RAxE11goTjDR0qYREs4sa4ps7kli_aNunR3OEX99GFB24130_provenance a np:Provenance .
  dgn-np:NP219956.RAxE11goTjDR0qYREs4sa4ps7kli_aNunR3OEX99GFB24130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP219956.RAxE11goTjDR0qYREs4sa4ps7kli_aNunR3OEX99GFB24130_assertion {
  miriam-gene:7490 a ncit:C16612 .
  lld:C0010417 a ncit:C7057 .
  dgn-gda:DGN760b49c4590a976fca6b48642d1907d3 sio:SIO_000628 miriam-gene:7490 , lld:C0010417 ;
    a sio:SIO_001121 .
}
dgn-np:NP219956.RAxE11goTjDR0qYREs4sa4ps7kli_aNunR3OEX99GFB24130_provenance {
  dgn-np:NP219956.RAxE11goTjDR0qYREs4sa4ps7kli_aNunR3OEX99GFB24130_assertion dcterms:description "[Mutations in the WT1 gene causing Wilms tumors were first reported in WAGR syndrome (Wilms tumor, Aniridia, Genitourinary malformation, mental Retardation) and Denys Drash syndrome (pseudohermaphroditism, Wilms tumor, nephropathy), but only in a few patients with hypospadias and cryptorchidism without other signs of Denys Drash (DDS) or WAGR syndrome WT1 mutations were identified.]. 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:10022588 ;
    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:NP219956.RAxE11goTjDR0qYREs4sa4ps7kli_aNunR3OEX99GFB24130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:02+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" .
}