@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP518257.RAP8Jx9yoEYtHKK4CqMDTfdu_B10FHBncl-Nqs9mldZfA> .
@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:NP518257.RAP8Jx9yoEYtHKK4CqMDTfdu_B10FHBncl-Nqs9mldZfA130_head {
   this: np:hasAssertion dgn-np:NP518257.RAP8Jx9yoEYtHKK4CqMDTfdu_B10FHBncl-Nqs9mldZfA130_assertion ;
    np:hasProvenance dgn-np:NP518257.RAP8Jx9yoEYtHKK4CqMDTfdu_B10FHBncl-Nqs9mldZfA130_provenance ;
    np:hasPublicationInfo dgn-np:NP518257.RAP8Jx9yoEYtHKK4CqMDTfdu_B10FHBncl-Nqs9mldZfA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP518257.RAP8Jx9yoEYtHKK4CqMDTfdu_B10FHBncl-Nqs9mldZfA130_assertion a np:Assertion .
  dgn-np:NP518257.RAP8Jx9yoEYtHKK4CqMDTfdu_B10FHBncl-Nqs9mldZfA130_provenance a np:Provenance .
  dgn-np:NP518257.RAP8Jx9yoEYtHKK4CqMDTfdu_B10FHBncl-Nqs9mldZfA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP518257.RAP8Jx9yoEYtHKK4CqMDTfdu_B10FHBncl-Nqs9mldZfA130_assertion {
   miriam-gene:4297 a ncit:C16612 .
  lld:C0280141 a ncit:C7057 .
  dgn-gda:DGN16fbdee00bed8a6008c2ff1b21c22566 sio:SIO_000628 miriam-gene:4297 , lld:C0280141 ;
    a sio:SIO_001121 .
}
dgn-np:NP518257.RAP8Jx9yoEYtHKK4CqMDTfdu_B10FHBncl-Nqs9mldZfA130_provenance {
   dgn-np:NP518257.RAP8Jx9yoEYtHKK4CqMDTfdu_B10FHBncl-Nqs9mldZfA130_assertion dcterms:description "[A WT1 mutation-associated gene-expression signature, reported here for the first time, included CD96, a leukemia stem cell-specific marker, and genes involved in gene regulation (eg, MLL, PML, and SNRPN) and in proliferative and metabolic processes (eg, INSR, IRS2, and PRKAA1), supporting the role of mutated WT1 in deregulating multiple homeostatic processes.]. 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:20442368 ;
    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:NP518257.RAP8Jx9yoEYtHKK4CqMDTfdu_B10FHBncl-Nqs9mldZfA130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:08+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" .
}