@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP420013.RA4dYqggNU7RezrOuowt2vr6gLzGiGHJbjvGBsi9O1FFU> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP420013.RA4dYqggNU7RezrOuowt2vr6gLzGiGHJbjvGBsi9O1FFU130_head {
  this: np:hasAssertion dgn-np:NP420013.RA4dYqggNU7RezrOuowt2vr6gLzGiGHJbjvGBsi9O1FFU130_assertion;
    np:hasProvenance dgn-np:NP420013.RA4dYqggNU7RezrOuowt2vr6gLzGiGHJbjvGBsi9O1FFU130_provenance;
    np:hasPublicationInfo dgn-np:NP420013.RA4dYqggNU7RezrOuowt2vr6gLzGiGHJbjvGBsi9O1FFU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP420013.RA4dYqggNU7RezrOuowt2vr6gLzGiGHJbjvGBsi9O1FFU130_assertion a np:Assertion .
  
  dgn-np:NP420013.RA4dYqggNU7RezrOuowt2vr6gLzGiGHJbjvGBsi9O1FFU130_provenance a np:Provenance .
  
  dgn-np:NP420013.RA4dYqggNU7RezrOuowt2vr6gLzGiGHJbjvGBsi9O1FFU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP420013.RA4dYqggNU7RezrOuowt2vr6gLzGiGHJbjvGBsi9O1FFU130_assertion {
  miriam-gene:2636 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGNe2525ddc1f6013626635a1c2ced43fa8 sio:SIO_000628 miriam-gene:2636, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP420013.RA4dYqggNU7RezrOuowt2vr6gLzGiGHJbjvGBsi9O1FFU130_provenance {
  dgn-np:NP420013.RA4dYqggNU7RezrOuowt2vr6gLzGiGHJbjvGBsi9O1FFU130_assertion dcterms:description
      "[Using RT-PCR, we screened members of the EHG family of homeobox genes, comprising EN1 (at 2q14), GBX2 (at 2q36), and EN2, GBX1, and HLXB9 (at 7q36), for dysregulation in acute myeloid leukemia (AML) cell lines indicated by chromosomal breakpoints at these sites.]. 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:15540222;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP420013.RA4dYqggNU7RezrOuowt2vr6gLzGiGHJbjvGBsi9O1FFU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:44+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}