@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP540363.RA_maikwVsbHGwdnulpy0qPiTtizXLi4mEInJSVEqzFDQ> .
@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:NP540363.RA_maikwVsbHGwdnulpy0qPiTtizXLi4mEInJSVEqzFDQ130_head {
  this: np:hasAssertion dgn-np:NP540363.RA_maikwVsbHGwdnulpy0qPiTtizXLi4mEInJSVEqzFDQ130_assertion;
    np:hasProvenance dgn-np:NP540363.RA_maikwVsbHGwdnulpy0qPiTtizXLi4mEInJSVEqzFDQ130_provenance;
    np:hasPublicationInfo dgn-np:NP540363.RA_maikwVsbHGwdnulpy0qPiTtizXLi4mEInJSVEqzFDQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP540363.RA_maikwVsbHGwdnulpy0qPiTtizXLi4mEInJSVEqzFDQ130_assertion a np:Assertion .
  
  dgn-np:NP540363.RA_maikwVsbHGwdnulpy0qPiTtizXLi4mEInJSVEqzFDQ130_provenance a np:Provenance .
  
  dgn-np:NP540363.RA_maikwVsbHGwdnulpy0qPiTtizXLi4mEInJSVEqzFDQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP540363.RA_maikwVsbHGwdnulpy0qPiTtizXLi4mEInJSVEqzFDQ130_assertion {
  miriam-gene:25 a ncit:C16612 .
  
  lld:C1333046 a ncit:C7057 .
  
  dgn-gda:DGNeee66afafea23225f9fa0770652f90bf sio:SIO_000628 miriam-gene:25, lld:C1333046;
    a sio:SIO_001121 .
}

dgn-np:NP540363.RA_maikwVsbHGwdnulpy0qPiTtizXLi4mEInJSVEqzFDQ130_provenance {
  dgn-np:NP540363.RA_maikwVsbHGwdnulpy0qPiTtizXLi4mEInJSVEqzFDQ130_assertion dcterms:description
      "[Recent years showed significant progress in the molecular characterization of the chronic myeloproliferative disorders (CMPD) which are classified according to the WHO classification of 2001 as polycythemia vera (PV), chronic idiopathic myelofibrosis (CIMF), essential thrombocythemia (ET), CMPD/unclassifiable (CMPD-U), chronic neutrophilic leukemia, and chronic eosinophilic leukemia (CEL)/hypereosinophilic syndrome, all to be delineated from BCR/ABL-positive chronic myeloid leukemia (CML).]. 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:17938925;
    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:NP540363.RA_maikwVsbHGwdnulpy0qPiTtizXLi4mEInJSVEqzFDQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:26+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" .
}