@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI> .
@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:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_head {
  this: np:hasAssertion dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_assertion ;
    np:hasProvenance dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_provenance ;
    np:hasPublicationInfo dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_assertion a np:Assertion .
  dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_provenance a np:Provenance .
  dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_assertion {
  miriam-gene:1056 a ncit:C16612 .
  lld:C0263662 a ncit:C7057 .
  dgn-gda:DGNc8e21becd663f07546bd9e6638d91d70 sio:SIO_000628 miriam-gene:1056 , lld:C0263662 ;
    a sio:SIO_001121 .
}
dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_provenance {
  dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_assertion dcterms:description "[Histological investigation in 31 chronic myeloid leukemia (CML), 29 CMPDs not otherwise specified (CMPD-NOS), 28 essential thrombocytosis (ET), 15 polycythemia vera (PV) and three chronic eosinophilic leukemia/hypereosinophilic syndrome (CEL/HES) exhibited in 32% various amounts of lymphocytic infiltrate of sparsely to moderately diffuse or nodular types in the bone marrow, but the reactive or coinciding lymphomatous nature could not be revealed by histology alone in the majority of cases.]. 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:15257312 ;
    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:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:21+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" .
}