@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ> .
@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:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_head {
  this: np:hasAssertion dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_assertion;
    np:hasProvenance dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_provenance;
    np:hasPublicationInfo dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_assertion a np:Assertion .
  
  dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_provenance a np:Provenance .
  
  dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_assertion {
  miriam-gene:2187 a ncit:C16612 .
  
  lld:C0023480 a ncit:C7057 .
  
  dgn-gda:DGNa7936a5d4f099d345cde53939c7cb488 sio:SIO_000628 miriam-gene:2187, lld:C0023480;
    a sio:SIO_001121 .
}

dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_provenance {
  dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_assertion dcterms:description
      "[Five patients had myelodysplastic syndrome (MDS) diagnosed according to the FAB nomenclature as chronic myelomonocytic leukemia (CMML) in two cases, refractory anemia with excess of blasts in transformation (RAEBt) in two cases, and refractory anemia with excess of blasts (RAEB) in one case.]. 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:2328318;
    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:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:18+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" .
}