@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP695831.RAIulNBsGAWwRMsRcooAT5fS6xOx8He6iP5v6-GCTEz3k> .
@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:NP695831.RAIulNBsGAWwRMsRcooAT5fS6xOx8He6iP5v6-GCTEz3k130_head {
  this: np:hasAssertion dgn-np:NP695831.RAIulNBsGAWwRMsRcooAT5fS6xOx8He6iP5v6-GCTEz3k130_assertion;
    np:hasProvenance dgn-np:NP695831.RAIulNBsGAWwRMsRcooAT5fS6xOx8He6iP5v6-GCTEz3k130_provenance;
    np:hasPublicationInfo dgn-np:NP695831.RAIulNBsGAWwRMsRcooAT5fS6xOx8He6iP5v6-GCTEz3k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP695831.RAIulNBsGAWwRMsRcooAT5fS6xOx8He6iP5v6-GCTEz3k130_assertion a np:Assertion .
  
  dgn-np:NP695831.RAIulNBsGAWwRMsRcooAT5fS6xOx8He6iP5v6-GCTEz3k130_provenance a np:Provenance .
  
  dgn-np:NP695831.RAIulNBsGAWwRMsRcooAT5fS6xOx8He6iP5v6-GCTEz3k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP695831.RAIulNBsGAWwRMsRcooAT5fS6xOx8He6iP5v6-GCTEz3k130_assertion {
  miriam-gene:4547 a ncit:C16612 .
  
  lld:C0598766 a ncit:C7057 .
  
  dgn-gda:DGNc3f29e50cb22a0c85a56db11c5a9f008 sio:SIO_000628 miriam-gene:4547, lld:C0598766;
    a sio:SIO_001121 .
}

dgn-np:NP695831.RAIulNBsGAWwRMsRcooAT5fS6xOx8He6iP5v6-GCTEz3k130_provenance {
  dgn-np:NP695831.RAIulNBsGAWwRMsRcooAT5fS6xOx8He6iP5v6-GCTEz3k130_assertion dcterms:description
      "[This is the first report of an ALL case with ABL amplification, and the authors speculate that both ABL proto-oncogene amplification and the p16(INK4a) tumor suppressor gene deletion have been implicated in leukemogenesis in the present case, although whether the ABL amplification truly contributes to the leukemogenesis or merely an epiphenomenon representing underlying genomic instability remains to be determined.]. 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:15282669;
    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:NP695831.RAIulNBsGAWwRMsRcooAT5fS6xOx8He6iP5v6-GCTEz3k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:03+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" .
}