@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I> .
@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/v3.0.0/void/> .

dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_head {
  this: np:hasAssertion dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_assertion;
    np:hasProvenance dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_provenance;
    np:hasPublicationInfo dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_assertion a np:Assertion .
  
  dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_provenance a np:Provenance .
  
  dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_assertion {
  miriam-gene:4928 a ncit:C16612 .
  
  lld:C0005699 a ncit:C7057 .
  
  dgn-gda:DGNb6017cdf0f97dbe33fd760791a0b9f77 sio:SIO_000628 miriam-gene:4928, lld:C0005699;
    a sio:SIO_001121 .
}

dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_provenance {
  dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_assertion dcterms:description
      "[NUP98 is known to be fused to at least 28 different partner genes in patients with hematopoietic malignancies, including acute myeloid leukemia, chronic myeloid leukemia in blast crisis, myelodysplastic syndrome, acute lymphoblastic leukemia, and bilineage/biphenotypic leukemia.]. 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:21948299;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:39+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}