@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP523644.RAjs8yoqm5VglqJypwtRHQKuyRvHTokMe9nO7EI3Ig0cI> .
@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:NP523644.RAjs8yoqm5VglqJypwtRHQKuyRvHTokMe9nO7EI3Ig0cI130_head {
  this: np:hasAssertion dgn-np:NP523644.RAjs8yoqm5VglqJypwtRHQKuyRvHTokMe9nO7EI3Ig0cI130_assertion;
    np:hasProvenance dgn-np:NP523644.RAjs8yoqm5VglqJypwtRHQKuyRvHTokMe9nO7EI3Ig0cI130_provenance;
    np:hasPublicationInfo dgn-np:NP523644.RAjs8yoqm5VglqJypwtRHQKuyRvHTokMe9nO7EI3Ig0cI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP523644.RAjs8yoqm5VglqJypwtRHQKuyRvHTokMe9nO7EI3Ig0cI130_assertion a np:Assertion .
  
  dgn-np:NP523644.RAjs8yoqm5VglqJypwtRHQKuyRvHTokMe9nO7EI3Ig0cI130_provenance a np:Provenance .
  
  dgn-np:NP523644.RAjs8yoqm5VglqJypwtRHQKuyRvHTokMe9nO7EI3Ig0cI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP523644.RAjs8yoqm5VglqJypwtRHQKuyRvHTokMe9nO7EI3Ig0cI130_assertion {
  miriam-gene:2187 a ncit:C16612 .
  
  lld:C1264195 a ncit:C7057 .
  
  dgn-gda:DGNe537befd994a93a26cc707bded61e9e8 sio:SIO_000628 miriam-gene:2187, lld:C1264195;
    a sio:SIO_001121 .
}

dgn-np:NP523644.RAjs8yoqm5VglqJypwtRHQKuyRvHTokMe9nO7EI3Ig0cI130_provenance {
  dgn-np:NP523644.RAjs8yoqm5VglqJypwtRHQKuyRvHTokMe9nO7EI3Ig0cI130_assertion dcterms:description
      "[Myelodysplastic syndromes (MDS) characterized by multilineage cytopenias and dysplasia but lacking an increase in blasts, with no Auer rods or monocytosis, do not exactly fit any of the categories of the French-American-British (FAB) classification of MDS and are often diagnosed as refractory anemia (RA), refractory anemia with ringed sideroblasts (RARS), or 'unclassifiable' MDS.]. 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:8558932;
    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:NP523644.RAjs8yoqm5VglqJypwtRHQKuyRvHTokMe9nO7EI3Ig0cI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:14+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" .
}