@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP502059.RA2ynpeF06TmIgRQzmsFTg2y7Q4qVuN0LI2v4Q3JqtcGc> .
@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:NP502059.RA2ynpeF06TmIgRQzmsFTg2y7Q4qVuN0LI2v4Q3JqtcGc130_head {
  this: np:hasAssertion dgn-np:NP502059.RA2ynpeF06TmIgRQzmsFTg2y7Q4qVuN0LI2v4Q3JqtcGc130_assertion ;
    np:hasProvenance dgn-np:NP502059.RA2ynpeF06TmIgRQzmsFTg2y7Q4qVuN0LI2v4Q3JqtcGc130_provenance ;
    np:hasPublicationInfo dgn-np:NP502059.RA2ynpeF06TmIgRQzmsFTg2y7Q4qVuN0LI2v4Q3JqtcGc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP502059.RA2ynpeF06TmIgRQzmsFTg2y7Q4qVuN0LI2v4Q3JqtcGc130_assertion a np:Assertion .
  dgn-np:NP502059.RA2ynpeF06TmIgRQzmsFTg2y7Q4qVuN0LI2v4Q3JqtcGc130_provenance a np:Provenance .
  dgn-np:NP502059.RA2ynpeF06TmIgRQzmsFTg2y7Q4qVuN0LI2v4Q3JqtcGc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP502059.RA2ynpeF06TmIgRQzmsFTg2y7Q4qVuN0LI2v4Q3JqtcGc130_assertion {
  miriam-gene:5966 a ncit:C16612 .
  lld:C0024299 a ncit:C7057 .
  dgn-gda:DGN3c51bb78dd1f2841712e3905cb8aaac9 sio:SIO_000628 miriam-gene:5966 , lld:C0024299 ;
    a sio:SIO_001121 .
}
dgn-np:NP502059.RA2ynpeF06TmIgRQzmsFTg2y7Q4qVuN0LI2v4Q3JqtcGc130_provenance {
  dgn-np:NP502059.RA2ynpeF06TmIgRQzmsFTg2y7Q4qVuN0LI2v4Q3JqtcGc130_assertion dcterms:description "[Reverse transcriptase-polymerase chain reaction analysis of mRNA from both primary lymphoma samples and several transformed tissue culture cell lines indicates that the RELDelta9 splice variant is preferentially expressed in lymphoma, suggesting that the REL transcript lacking exon 9 could serve as a marker for certain types of lymphoid tumors.]. 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:18695674 ;
    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:NP502059.RA2ynpeF06TmIgRQzmsFTg2y7Q4qVuN0LI2v4Q3JqtcGc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:59+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" .
}