@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP793232.RAVRYeVTYXNJd4-It66R-MtOQL4BrjECjG9ME8kYIxhIM> .
@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:NP793232.RAVRYeVTYXNJd4-It66R-MtOQL4BrjECjG9ME8kYIxhIM130_head {
  this: np:hasAssertion dgn-np:NP793232.RAVRYeVTYXNJd4-It66R-MtOQL4BrjECjG9ME8kYIxhIM130_assertion;
    np:hasProvenance dgn-np:NP793232.RAVRYeVTYXNJd4-It66R-MtOQL4BrjECjG9ME8kYIxhIM130_provenance;
    np:hasPublicationInfo dgn-np:NP793232.RAVRYeVTYXNJd4-It66R-MtOQL4BrjECjG9ME8kYIxhIM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP793232.RAVRYeVTYXNJd4-It66R-MtOQL4BrjECjG9ME8kYIxhIM130_assertion a np:Assertion .
  
  dgn-np:NP793232.RAVRYeVTYXNJd4-It66R-MtOQL4BrjECjG9ME8kYIxhIM130_provenance a np:Provenance .
  
  dgn-np:NP793232.RAVRYeVTYXNJd4-It66R-MtOQL4BrjECjG9ME8kYIxhIM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP793232.RAVRYeVTYXNJd4-It66R-MtOQL4BrjECjG9ME8kYIxhIM130_assertion {
  miriam-gene:8233 a ncit:C16612 .
  
  lld:C0026986 a ncit:C7057 .
  
  dgn-gda:DGN299234356b6ec3153c22df8dba70be09 sio:SIO_000628 miriam-gene:8233, lld:C0026986;
    a sio:SIO_001121 .
}

dgn-np:NP793232.RAVRYeVTYXNJd4-It66R-MtOQL4BrjECjG9ME8kYIxhIM130_provenance {
  dgn-np:NP793232.RAVRYeVTYXNJd4-It66R-MtOQL4BrjECjG9ME8kYIxhIM130_assertion dcterms:description
      "[Recent studies are shedding light on the molecular basis of myelodysplasia and how mutations and epimutations can induce and promote this neoplastic process through aberrant transcription factor function (RUNX1, ETV6, TP53), kinase signalling (FLT3, NRAS, KIT, CBL) and epigenetic deregulation (TET2, IDH1/2, DNMT3A, EZH2, ASXL1, SF3B1, U2AF1, SRSF2, ZRSR2).]. 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:24903747;
    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:NP793232.RAVRYeVTYXNJd4-It66R-MtOQL4BrjECjG9ME8kYIxhIM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:39+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" .
}