@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U> .
@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:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_head {
  this: np:hasAssertion dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_assertion;
    np:hasProvenance dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_provenance;
    np:hasPublicationInfo dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_assertion a np:Assertion .
  
  dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_provenance a np:Provenance .
  
  dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_assertion {
  miriam-gene:861 a ncit:C16612 .
  
  lld:C0033027 a ncit:C7057 .
  
  dgn-gda:DGNff0836e6a2359c6128bed8b15fba8e8f sio:SIO_000628 miriam-gene:861, lld:C0033027;
    a sio:SIO_001121 .
}

dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_provenance {
  dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_assertion dcterms:description
      "[Somatic mutation of the AML1/RUNX1(RUNX1) gene is seen in acute myeloid leukemia (AML) M0 subtype and in AML transformed from myelodysplastic syndrome, but the impact of this gene mutation on survival in AML patients remains unclear.]. 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:19808697;
    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:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:01+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" .
}