@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ> .
@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:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_head {
  this: np:hasAssertion dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_assertion;
    np:hasProvenance dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_provenance;
    np:hasPublicationInfo dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_assertion a np:Assertion .
  
  dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_provenance a np:Provenance .
  
  dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_assertion {
  miriam-gene:861 a ncit:C16612 .
  
  lld:C0002894 a ncit:C7057 .
  
  dgn-gda:DGNbcb6eb6f49f710275163c9608cc73b6b sio:SIO_000628 miriam-gene:861, lld:C0002894;
    a sio:SIO_001121 .
}

dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_provenance {
  dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_assertion dcterms:description
      "[AML1/RUNX1 mutations have been reported frequently in myelodysplastic syndrome (MDS) patients, especially those diagnosed with refractory anemia with excess blast (RAEB), RAEB in transformation (RAEBt), or AML following MDS (these categories are defined as MDS/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:16467864;
    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:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:05+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" .
}