@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP225187.RAEPVlvD4370NEdudVQigDAeN0cMAS3WkDFEtBgJV-keM> .
@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:NP225187.RAEPVlvD4370NEdudVQigDAeN0cMAS3WkDFEtBgJV-keM130_head {
  this: np:hasAssertion dgn-np:NP225187.RAEPVlvD4370NEdudVQigDAeN0cMAS3WkDFEtBgJV-keM130_assertion;
    np:hasProvenance dgn-np:NP225187.RAEPVlvD4370NEdudVQigDAeN0cMAS3WkDFEtBgJV-keM130_provenance;
    np:hasPublicationInfo dgn-np:NP225187.RAEPVlvD4370NEdudVQigDAeN0cMAS3WkDFEtBgJV-keM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP225187.RAEPVlvD4370NEdudVQigDAeN0cMAS3WkDFEtBgJV-keM130_assertion a np:Assertion .
  
  dgn-np:NP225187.RAEPVlvD4370NEdudVQigDAeN0cMAS3WkDFEtBgJV-keM130_provenance a np:Provenance .
  
  dgn-np:NP225187.RAEPVlvD4370NEdudVQigDAeN0cMAS3WkDFEtBgJV-keM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP225187.RAEPVlvD4370NEdudVQigDAeN0cMAS3WkDFEtBgJV-keM130_assertion {
  miriam-gene:3092 a ncit:C16612 .
  
  lld:C0376544 a ncit:C7057 .
  
  dgn-gda:DGN7a26fac2e4ec2540c6e6ad54c5f6d66f sio:SIO_000628 miriam-gene:3092, lld:C0376544;
    a sio:SIO_001121 .
}

dgn-np:NP225187.RAEPVlvD4370NEdudVQigDAeN0cMAS3WkDFEtBgJV-keM130_provenance {
  dgn-np:NP225187.RAEPVlvD4370NEdudVQigDAeN0cMAS3WkDFEtBgJV-keM130_assertion dcterms:description
      "[These data are consistent with an alternative mechanism for activation of PDGFbetaR tyrosine kinase activity by fusion with HIP1, leading to transformation of hematopoietic cells, and may implicate Huntingtin or HIP1 in the pathogenesis of hematopoietic malignancies.]. 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:9616134;
    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:NP225187.RAEPVlvD4370NEdudVQigDAeN0cMAS3WkDFEtBgJV-keM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:05+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" .
}