@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns> .
@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:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_head {
  this: np:hasAssertion dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_assertion;
    np:hasProvenance dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_provenance;
    np:hasPublicationInfo dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_assertion a np:Assertion .
  
  dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_provenance a np:Provenance .
  
  dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_assertion {
  miriam-gene:2125 a ncit:C16612 .
  
  lld:C0598766 a ncit:C7057 .
  
  dgn-gda:DGNfed42c5a93b057d2947dfe2c556f1016 sio:SIO_000628 miriam-gene:2125, lld:C0598766;
    a sio:SIO_001121 .
}

dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_provenance {
  dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_assertion dcterms:description
      "[The e1a2, b2a2 or b3a2 and c3a2 fusion mRNAs encode distinct fusion proteins (p190, p210 and p230, respectively), which are associated with different forms of leukemogenesis in humans and animal models.]. 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:10602422;
    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:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:27+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" .
}