@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps> .
@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:NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_head {
  this: np:hasAssertion dgn-np:NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_assertion ;
    np:hasProvenance dgn-np:NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_provenance ;
    np:hasPublicationInfo dgn-np:NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_assertion a np:Assertion .
  dgn-np:NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_provenance a np:Provenance .
  dgn-np:NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_assertion {
  miriam-gene:1869 a ncit:C16612 .
  lld:C0026985 a ncit:C7057 .
  dgn-gda:DGN1e28244f16ca82ee0e91cb9f0f12258c sio:SIO_000628 miriam-gene:1869 , lld:C0026985 ;
    a sio:SIO_001121 .
}
dgn-np:NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_provenance {
  dgn-np:NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_assertion dcterms:description "[Although deletions or structural rearrangements of E2F1 were not detected in 14 primary acute leukemia or myelodysplasia samples with structural abnormalities of chromosome 20q11, the gene was amplified and overexpressed in HEL erythroleukemia cells and translocated to other chromosomes in several established human leukemia cell lines.]. 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:7774910 ;
    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:NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:36+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" .
}