@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI> .
@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:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_head {
  this: np:hasAssertion dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_assertion ;
    np:hasProvenance dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_provenance ;
    np:hasPublicationInfo dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_assertion a np:Assertion .
  dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_provenance a np:Provenance .
  dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_assertion {
  miriam-gene:4211 a ncit:C16612 .
  lld:C0023418 a ncit:C7057 .
  dgn-gda:DGN79a3708bbb9d83ecf708f5e6f5c10be1 sio:SIO_000628 miriam-gene:4211 , lld:C0023418 ;
    a sio:SIO_001121 .
}
dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_provenance {
  dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_assertion dcterms:description "[Phylogenetic sequence analysis and reporter assays in MEIS1-expressing (K562) and nonexpressing (HL60) leukemic cell line models were used to identify key regulatory regions and potential transcription factor binding sites within the candidate promoter region followed by functional and expression studies of one identified regulator in both cell lines and primary human cord blood and leukemia samples.]. 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:20600580 ;
    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:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:41+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" .
}