@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc> .
@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:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_head {
  this: np:hasAssertion dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_assertion;
    np:hasProvenance dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_provenance;
    np:hasPublicationInfo dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_assertion a np:Assertion .
  
  dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_provenance a np:Provenance .
  
  dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_assertion {
  miriam-gene:7294 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGN6094d2fc4d6299b6d4c5bc756045b54b sio:SIO_000628 miriam-gene:7294, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_provenance {
  dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_assertion dcterms:description
      "[Activating FLT3 mutations are the most common genetic aberrations in acute myeloid leukemia (AML), resulting in the constitutive activation of this receptor tyrosine kinase (RTK), but such mutations are rarely found in acute lymphoblastic leukemia (ALL).]. 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:15044257;
    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:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:05+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" .
}