@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP975225.RAiTnSDWeQI2ev9vju1lKMXsr_xT9A98LYSPhGAfNSQEE> .
@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/v4.0.0/void/> .

dgn-np:NP975225.RAiTnSDWeQI2ev9vju1lKMXsr_xT9A98LYSPhGAfNSQEE130_head {
  this: np:hasAssertion dgn-np:NP975225.RAiTnSDWeQI2ev9vju1lKMXsr_xT9A98LYSPhGAfNSQEE130_assertion;
    np:hasProvenance dgn-np:NP975225.RAiTnSDWeQI2ev9vju1lKMXsr_xT9A98LYSPhGAfNSQEE130_provenance;
    np:hasPublicationInfo dgn-np:NP975225.RAiTnSDWeQI2ev9vju1lKMXsr_xT9A98LYSPhGAfNSQEE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP975225.RAiTnSDWeQI2ev9vju1lKMXsr_xT9A98LYSPhGAfNSQEE130_assertion a np:Assertion .
  
  dgn-np:NP975225.RAiTnSDWeQI2ev9vju1lKMXsr_xT9A98LYSPhGAfNSQEE130_provenance a np:Provenance .
  
  dgn-np:NP975225.RAiTnSDWeQI2ev9vju1lKMXsr_xT9A98LYSPhGAfNSQEE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP975225.RAiTnSDWeQI2ev9vju1lKMXsr_xT9A98LYSPhGAfNSQEE130_assertion {
  miriam-gene:2322 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGN94669eff562ea0be6abd79517db0c264 sio:SIO_000628 miriam-gene:2322, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP975225.RAiTnSDWeQI2ev9vju1lKMXsr_xT9A98LYSPhGAfNSQEE130_provenance {
  dgn-np:NP975225.RAiTnSDWeQI2ev9vju1lKMXsr_xT9A98LYSPhGAfNSQEE130_assertion dcterms:description
      "[Nonetheless, mutations in DNMT3A, TET2, and ASXL1 are emerging as important adverse prognosticators in subsets of patients with AML independent of FLT3 mutations whereas mutations in IDH2 at residue 140 are potential predictors of improved outcome in 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:22507776;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP975225.RAiTnSDWeQI2ev9vju1lKMXsr_xT9A98LYSPhGAfNSQEE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:06+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}