@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP597531.RAeKaeXXbtPfBShmAvwTDhhpvYV7jEx1Ak1-geiPjOqII> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP597531.RAeKaeXXbtPfBShmAvwTDhhpvYV7jEx1Ak1-geiPjOqII130_head {
  this: np:hasAssertion dgn-np:NP597531.RAeKaeXXbtPfBShmAvwTDhhpvYV7jEx1Ak1-geiPjOqII130_assertion;
    np:hasProvenance dgn-np:NP597531.RAeKaeXXbtPfBShmAvwTDhhpvYV7jEx1Ak1-geiPjOqII130_provenance;
    np:hasPublicationInfo dgn-np:NP597531.RAeKaeXXbtPfBShmAvwTDhhpvYV7jEx1Ak1-geiPjOqII130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP597531.RAeKaeXXbtPfBShmAvwTDhhpvYV7jEx1Ak1-geiPjOqII130_assertion a np:Assertion .
  
  dgn-np:NP597531.RAeKaeXXbtPfBShmAvwTDhhpvYV7jEx1Ak1-geiPjOqII130_provenance a np:Provenance .
  
  dgn-np:NP597531.RAeKaeXXbtPfBShmAvwTDhhpvYV7jEx1Ak1-geiPjOqII130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP597531.RAeKaeXXbtPfBShmAvwTDhhpvYV7jEx1Ak1-geiPjOqII130_assertion {
  miriam-gene:4869 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGNfdeda2edb5f47f7fe036cf11967220ec sio:SIO_000628 miriam-gene:4869, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP597531.RAeKaeXXbtPfBShmAvwTDhhpvYV7jEx1Ak1-geiPjOqII130_provenance {
  dgn-np:NP597531.RAeKaeXXbtPfBShmAvwTDhhpvYV7jEx1Ak1-geiPjOqII130_assertion dcterms:description
      "[WT1 overexpression by itself is an independent and negative indicator for predicting CR rate, DFS and OS of the CN-AML patients; moreover, it increases the statistical power of predicting the same clinical outcomes when it is combined with the NPM1(mt) or the FLT3(ITD) genotypes that are the good or poor prognostic markers of CN-AML.]. 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:24667279;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP597531.RAeKaeXXbtPfBShmAvwTDhhpvYV7jEx1Ak1-geiPjOqII130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:37+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}