@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP439127.RAveUHaFFqSpXvJVd8pPlBLZglD9R4wNSECrdMQZ8kPWE> .
@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:NP439127.RAveUHaFFqSpXvJVd8pPlBLZglD9R4wNSECrdMQZ8kPWE130_head {
  this: np:hasAssertion dgn-np:NP439127.RAveUHaFFqSpXvJVd8pPlBLZglD9R4wNSECrdMQZ8kPWE130_assertion;
    np:hasProvenance dgn-np:NP439127.RAveUHaFFqSpXvJVd8pPlBLZglD9R4wNSECrdMQZ8kPWE130_provenance;
    np:hasPublicationInfo dgn-np:NP439127.RAveUHaFFqSpXvJVd8pPlBLZglD9R4wNSECrdMQZ8kPWE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP439127.RAveUHaFFqSpXvJVd8pPlBLZglD9R4wNSECrdMQZ8kPWE130_assertion a np:Assertion .
  
  dgn-np:NP439127.RAveUHaFFqSpXvJVd8pPlBLZglD9R4wNSECrdMQZ8kPWE130_provenance a np:Provenance .
  
  dgn-np:NP439127.RAveUHaFFqSpXvJVd8pPlBLZglD9R4wNSECrdMQZ8kPWE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP439127.RAveUHaFFqSpXvJVd8pPlBLZglD9R4wNSECrdMQZ8kPWE130_assertion {
  miriam-gene:2122 a ncit:C16612 .
  
  lld:C0023470 a ncit:C7057 .
  
  dgn-gda:DGN5ff70f9fe0ecf2d1859f5163bb6ca39a sio:SIO_000628 miriam-gene:2122, lld:C0023470;
    a sio:SIO_001121 .
}

dgn-np:NP439127.RAveUHaFFqSpXvJVd8pPlBLZglD9R4wNSECrdMQZ8kPWE130_provenance {
  dgn-np:NP439127.RAveUHaFFqSpXvJVd8pPlBLZglD9R4wNSECrdMQZ8kPWE130_assertion dcterms:description
      "[In contrast to MDS1/EVI1, EVI1 is often activated inappropriately by chromosomal rearrangements at 3q26 leading to inappropriate expression of the protein in hematopoietic cells and to myeloid leukemias, which are often characterized by abnormal megakaryopoiesis.]. 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:10557037;
    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:NP439127.RAveUHaFFqSpXvJVd8pPlBLZglD9R4wNSECrdMQZ8kPWE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:20+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" .
}