@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP588987.RAJxa3AAOnipH7c4WMqC7BKotyf2_I_oEmRSK4J5SjWMM> .
@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:NP588987.RAJxa3AAOnipH7c4WMqC7BKotyf2_I_oEmRSK4J5SjWMM130_head {
  this: np:hasAssertion dgn-np:NP588987.RAJxa3AAOnipH7c4WMqC7BKotyf2_I_oEmRSK4J5SjWMM130_assertion;
    np:hasProvenance dgn-np:NP588987.RAJxa3AAOnipH7c4WMqC7BKotyf2_I_oEmRSK4J5SjWMM130_provenance;
    np:hasPublicationInfo dgn-np:NP588987.RAJxa3AAOnipH7c4WMqC7BKotyf2_I_oEmRSK4J5SjWMM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP588987.RAJxa3AAOnipH7c4WMqC7BKotyf2_I_oEmRSK4J5SjWMM130_assertion a np:Assertion .
  
  dgn-np:NP588987.RAJxa3AAOnipH7c4WMqC7BKotyf2_I_oEmRSK4J5SjWMM130_provenance a np:Provenance .
  
  dgn-np:NP588987.RAJxa3AAOnipH7c4WMqC7BKotyf2_I_oEmRSK4J5SjWMM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP588987.RAJxa3AAOnipH7c4WMqC7BKotyf2_I_oEmRSK4J5SjWMM130_assertion {
  miriam-gene:2623 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGN4cbac9c2aa97aac361f6c2728ef15aff sio:SIO_000628 miriam-gene:2623, lld:C0013080;
    a sio:SIO_001121 .
}

dgn-np:NP588987.RAJxa3AAOnipH7c4WMqC7BKotyf2_I_oEmRSK4J5SjWMM130_provenance {
  dgn-np:NP588987.RAJxa3AAOnipH7c4WMqC7BKotyf2_I_oEmRSK4J5SjWMM130_assertion dcterms:description
      "[Four years ago it was discovered that nearly all cases of transient myeloproliferative disorder and acute megakaryocytic leukemia in children with Down syndrome acquire mutations in the hematopoietic transcription factor gene GATA1.]. 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:17224656;
    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:NP588987.RAJxa3AAOnipH7c4WMqC7BKotyf2_I_oEmRSK4J5SjWMM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:12+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" .
}