@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59306.RAVm6RmxSmhh9O2f5-AiKwyXjCedQqsC9iwQAvkXa_MKw> .
@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:NP59306.RAVm6RmxSmhh9O2f5-AiKwyXjCedQqsC9iwQAvkXa_MKw130_head {
  this: np:hasAssertion dgn-np:NP59306.RAVm6RmxSmhh9O2f5-AiKwyXjCedQqsC9iwQAvkXa_MKw130_assertion ;
    np:hasProvenance dgn-np:NP59306.RAVm6RmxSmhh9O2f5-AiKwyXjCedQqsC9iwQAvkXa_MKw130_provenance ;
    np:hasPublicationInfo dgn-np:NP59306.RAVm6RmxSmhh9O2f5-AiKwyXjCedQqsC9iwQAvkXa_MKw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP59306.RAVm6RmxSmhh9O2f5-AiKwyXjCedQqsC9iwQAvkXa_MKw130_assertion a np:Assertion .
  dgn-np:NP59306.RAVm6RmxSmhh9O2f5-AiKwyXjCedQqsC9iwQAvkXa_MKw130_provenance a np:Provenance .
  dgn-np:NP59306.RAVm6RmxSmhh9O2f5-AiKwyXjCedQqsC9iwQAvkXa_MKw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP59306.RAVm6RmxSmhh9O2f5-AiKwyXjCedQqsC9iwQAvkXa_MKw130_assertion {
  miriam-gene:7490 a ncit:C16612 .
  lld:C0027726 a ncit:C7057 .
  dgn-gda:DGNce004713e98ee4783878cc903b2f8ed9 sio:SIO_000628 miriam-gene:7490 , lld:C0027726 ;
    a sio:SIO_001122 .
}
dgn-np:NP59306.RAVm6RmxSmhh9O2f5-AiKwyXjCedQqsC9iwQAvkXa_MKw130_provenance {
  dgn-np:NP59306.RAVm6RmxSmhh9O2f5-AiKwyXjCedQqsC9iwQAvkXa_MKw130_assertion dcterms:description "[ According to the data acquired in this study, patients presenting with a female phenotype and SRNS and male patients presenting with genital abnormalities should especially be screened to take advantage of the important genetic information on potential Wilms' tumor risk and differential therapy. This will also help to provide more data on the phenotype/genotype correlation in this patient population.]. 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:15253707 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP59306.RAVm6RmxSmhh9O2f5-AiKwyXjCedQqsC9iwQAvkXa_MKw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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: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" .
}