@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE> .
@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/v4.0.0/void/> .

dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_head {
  this: np:hasAssertion dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_assertion;
    np:hasProvenance dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_provenance;
    np:hasPublicationInfo dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_assertion a np:Assertion .
  
  dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_provenance a np:Provenance .
  
  dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_assertion {
  miriam-gene:2623 a ncit:C16612 .
  
  lld:C1834582 a ncit:C7057 .
  
  dgn-gda:DGNdd812ba0ad5d1ef201af317e21e9123d sio:SIO_000628 miriam-gene:2623, lld:C1834582;
    a sio:SIO_001121 .
}

dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_provenance {
  dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_assertion dcterms:description
      "[Recently, acquired mutations in the megakaryocytic regulator GATA1 have been found in essentially all cases of acute megakaryoblastic leukemia (AMkL) in children with Down syndrome and in the closely related malignancy transient myeloproliferative disorder.]. 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:16840187;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:58+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}