@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20> .
@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:NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_head {
  this: np:hasAssertion dgn-np:NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_assertion;
    np:hasProvenance dgn-np:NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance;
    np:hasPublicationInfo dgn-np:NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_assertion a np:Assertion .
  
  dgn-np:NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance a np:Provenance .
  
  dgn-np:NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_assertion {
  miriam-gene:4869 a ncit:C16612 .
  
  lld:C0026986 a ncit:C7057 .
  
  dgn-gda:DGN31b424d8a9fd06c4bd45203fbc4ec9d5 sio:SIO_000628 miriam-gene:4869, lld:C0026986;
    a sio:SIO_001122 .
}

dgn-np:NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_provenance {
  dgn-np:NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_assertion dcterms:description
      "[We examined 193 patients with myelodysplastic syndromes and 53 patients with acute myeloid leukemia arising from myelodysplastic syndromes for mutations in IDH1 (R132), IDH2 (R172 and R140), and NPM1 by direct sequencing.]. 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:20494930;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP90059.RAADrTFLSultwom4kRjECRUG_-r_2PyTTHsYKt2SZTF20130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:29+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" .
}