@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP351669.RAbiZ87jvqQ2tWl4u1WlE0ez6gu6Pt0EexTEWJ1N7_7L0> .
@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:NP351669.RAbiZ87jvqQ2tWl4u1WlE0ez6gu6Pt0EexTEWJ1N7_7L0130_head {
  this: np:hasAssertion dgn-np:NP351669.RAbiZ87jvqQ2tWl4u1WlE0ez6gu6Pt0EexTEWJ1N7_7L0130_assertion;
    np:hasProvenance dgn-np:NP351669.RAbiZ87jvqQ2tWl4u1WlE0ez6gu6Pt0EexTEWJ1N7_7L0130_provenance;
    np:hasPublicationInfo dgn-np:NP351669.RAbiZ87jvqQ2tWl4u1WlE0ez6gu6Pt0EexTEWJ1N7_7L0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP351669.RAbiZ87jvqQ2tWl4u1WlE0ez6gu6Pt0EexTEWJ1N7_7L0130_assertion a np:Assertion .
  
  dgn-np:NP351669.RAbiZ87jvqQ2tWl4u1WlE0ez6gu6Pt0EexTEWJ1N7_7L0130_provenance a np:Provenance .
  
  dgn-np:NP351669.RAbiZ87jvqQ2tWl4u1WlE0ez6gu6Pt0EexTEWJ1N7_7L0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP351669.RAbiZ87jvqQ2tWl4u1WlE0ez6gu6Pt0EexTEWJ1N7_7L0130_assertion {
  miriam-gene:7490 a ncit:C16612 .
  
  lld:C0206115 a ncit:C7057 .
  
  dgn-gda:DGN5711fc3a5a3134a15f8c24414feac5af sio:SIO_000628 miriam-gene:7490, lld:C0206115;
    a sio:SIO_001121 .
}

dgn-np:NP351669.RAbiZ87jvqQ2tWl4u1WlE0ez6gu6Pt0EexTEWJ1N7_7L0130_provenance {
  dgn-np:NP351669.RAbiZ87jvqQ2tWl4u1WlE0ez6gu6Pt0EexTEWJ1N7_7L0130_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:NP351669.RAbiZ87jvqQ2tWl4u1WlE0ez6gu6Pt0EexTEWJ1N7_7L0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:26+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" .
}