@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP852941.RAvSbCCTJMXoE6EIkinFUHObGoQyjVnMXiRcRCJT13OwA> .
@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:NP852941.RAvSbCCTJMXoE6EIkinFUHObGoQyjVnMXiRcRCJT13OwA130_head {
  this: np:hasAssertion dgn-np:NP852941.RAvSbCCTJMXoE6EIkinFUHObGoQyjVnMXiRcRCJT13OwA130_assertion;
    np:hasProvenance dgn-np:NP852941.RAvSbCCTJMXoE6EIkinFUHObGoQyjVnMXiRcRCJT13OwA130_provenance;
    np:hasPublicationInfo dgn-np:NP852941.RAvSbCCTJMXoE6EIkinFUHObGoQyjVnMXiRcRCJT13OwA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP852941.RAvSbCCTJMXoE6EIkinFUHObGoQyjVnMXiRcRCJT13OwA130_assertion a np:Assertion .
  
  dgn-np:NP852941.RAvSbCCTJMXoE6EIkinFUHObGoQyjVnMXiRcRCJT13OwA130_provenance a np:Provenance .
  
  dgn-np:NP852941.RAvSbCCTJMXoE6EIkinFUHObGoQyjVnMXiRcRCJT13OwA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP852941.RAvSbCCTJMXoE6EIkinFUHObGoQyjVnMXiRcRCJT13OwA130_assertion {
  miriam-gene:2623 a ncit:C16612 .
  
  lld:C0023462 a ncit:C7057 .
  
  dgn-gda:DGN3c6c40911a3a90cfc47404ce402744d8 sio:SIO_000628 miriam-gene:2623, lld:C0023462;
    a sio:SIO_001121 .
}

dgn-np:NP852941.RAvSbCCTJMXoE6EIkinFUHObGoQyjVnMXiRcRCJT13OwA130_provenance {
  dgn-np:NP852941.RAvSbCCTJMXoE6EIkinFUHObGoQyjVnMXiRcRCJT13OwA130_assertion dcterms:description
      "[Notable among DS children with acute myeloid leukemia (AML), is the high frequency of the acute megakaryocytic leukemia (AMkL) subtype, which uniformly harbor somatic mutations in the transcription factor GATA1 gene.]. 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:21083461;
    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:NP852941.RAvSbCCTJMXoE6EIkinFUHObGoQyjVnMXiRcRCJT13OwA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:11+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" .
}