@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow> .
@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:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_head {
  this: np:hasAssertion dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_assertion;
    np:hasProvenance dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_provenance;
    np:hasPublicationInfo dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_assertion a np:Assertion .
  
  dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_provenance a np:Provenance .
  
  dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_assertion {
  miriam-gene:3612 a ncit:C16612 .
  
  lld:C0349640 a ncit:C7057 .
  
  dgn-gda:DGN5564261431268176deeba44a02ade6d2 sio:SIO_000628 miriam-gene:3612, lld:C0349640;
    a sio:SIO_001121 .
}

dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_provenance {
  dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_assertion dcterms:description
      "[Using four criteria (monocytosis, percentage of IMP, basophilia, and percentage of erythroblasts in BM), patients could be divided into typical and atypical CML and this classification correlated well with molecular findings.]. 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:2070054;
    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:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:19+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" .
}