@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP166146.RAo4VpGWDn3QQAReWeylLRpA4CAaKx-DYEok3Ki479GFw> .
@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:NP166146.RAo4VpGWDn3QQAReWeylLRpA4CAaKx-DYEok3Ki479GFw130_head {
  this: np:hasAssertion dgn-np:NP166146.RAo4VpGWDn3QQAReWeylLRpA4CAaKx-DYEok3Ki479GFw130_assertion;
    np:hasProvenance dgn-np:NP166146.RAo4VpGWDn3QQAReWeylLRpA4CAaKx-DYEok3Ki479GFw130_provenance;
    np:hasPublicationInfo dgn-np:NP166146.RAo4VpGWDn3QQAReWeylLRpA4CAaKx-DYEok3Ki479GFw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP166146.RAo4VpGWDn3QQAReWeylLRpA4CAaKx-DYEok3Ki479GFw130_assertion a np:Assertion .
  
  dgn-np:NP166146.RAo4VpGWDn3QQAReWeylLRpA4CAaKx-DYEok3Ki479GFw130_provenance a np:Provenance .
  
  dgn-np:NP166146.RAo4VpGWDn3QQAReWeylLRpA4CAaKx-DYEok3Ki479GFw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP166146.RAo4VpGWDn3QQAReWeylLRpA4CAaKx-DYEok3Ki479GFw130_assertion {
  miriam-gene:7015 a ncit:C16612 .
  
  lld:C0023473 a ncit:C7057 .
  
  dgn-gda:DGNf8f10b5e872095f24647d87e9da67775 sio:SIO_000628 miriam-gene:7015, lld:C0023473;
    a sio:SIO_001121 .
}

dgn-np:NP166146.RAo4VpGWDn3QQAReWeylLRpA4CAaKx-DYEok3Ki479GFw130_provenance {
  dgn-np:NP166146.RAo4VpGWDn3QQAReWeylLRpA4CAaKx-DYEok3Ki479GFw130_assertion dcterms:description
      "[We could demonstrate that hTERT is differentially expressed in various haematologic stem cell disorders with significant higher levels in refractory anemia (RA) and chronic myeloid leukemia (CML) compared to other haematopoietic stem cell disorders and non-neoplastic haematopoiesis which may be used as a prognostic indicator in these entities.]. 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:15068898;
    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:NP166146.RAo4VpGWDn3QQAReWeylLRpA4CAaKx-DYEok3Ki479GFw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:30+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" .
}