@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP832235.RAcGv-Ra97438_F1DlSG5BvZxHTWGWNliSdHPuBYq7Y8k> .
@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:NP832235.RAcGv-Ra97438_F1DlSG5BvZxHTWGWNliSdHPuBYq7Y8k130_head {
  this: np:hasAssertion dgn-np:NP832235.RAcGv-Ra97438_F1DlSG5BvZxHTWGWNliSdHPuBYq7Y8k130_assertion;
    np:hasProvenance dgn-np:NP832235.RAcGv-Ra97438_F1DlSG5BvZxHTWGWNliSdHPuBYq7Y8k130_provenance;
    np:hasPublicationInfo dgn-np:NP832235.RAcGv-Ra97438_F1DlSG5BvZxHTWGWNliSdHPuBYq7Y8k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP832235.RAcGv-Ra97438_F1DlSG5BvZxHTWGWNliSdHPuBYq7Y8k130_assertion a np:Assertion .
  
  dgn-np:NP832235.RAcGv-Ra97438_F1DlSG5BvZxHTWGWNliSdHPuBYq7Y8k130_provenance a np:Provenance .
  
  dgn-np:NP832235.RAcGv-Ra97438_F1DlSG5BvZxHTWGWNliSdHPuBYq7Y8k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP832235.RAcGv-Ra97438_F1DlSG5BvZxHTWGWNliSdHPuBYq7Y8k130_assertion {
  miriam-gene:3110 a ncit:C16612 .
  
  lld:C0598766 a ncit:C7057 .
  
  dgn-gda:DGN38f8ba3477312db562c681e6d25051a9 sio:SIO_000628 miriam-gene:3110, lld:C0598766;
    a sio:SIO_001121 .
}

dgn-np:NP832235.RAcGv-Ra97438_F1DlSG5BvZxHTWGWNliSdHPuBYq7Y8k130_provenance {
  dgn-np:NP832235.RAcGv-Ra97438_F1DlSG5BvZxHTWGWNliSdHPuBYq7Y8k130_assertion dcterms:description
      "[These findings demonstrate that high levels of HB9 and HB24 expression are common features of acute leukemia and suggest the possibility that the dysregulated expression of these two genes may contribute to leukemogenesis.]. 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:7680402;
    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:NP832235.RAcGv-Ra97438_F1DlSG5BvZxHTWGWNliSdHPuBYq7Y8k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:29+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" .
}