@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_head {
  this: np:hasAssertion dgn-np:NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_assertion ;
    np:hasProvenance dgn-np:NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_provenance ;
    np:hasPublicationInfo dgn-np:NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_assertion a np:Assertion .
  dgn-np:NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_provenance a np:Provenance .
  dgn-np:NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  lld:C0032463 a ncit:C7057 .
  dgn-gda:DGN7cd65763cf39937e4685235677591bad sio:SIO_000628 miriam-gene:3717 , lld:C0032463 ;
    a sio:SIO_001122 .
}
dgn-np:NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_provenance {
  dgn-np:NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_assertion dcterms:description "[The high prevalence of the V617F mutation of Janus kinase 2 and associated mutations in myeloproliferative disorders (&gt; 95% in polycythemia vera and about half of patients with essential thrombocythemia and primary myelofibrosis) has led the World Health Organization to alter the diagnostic criteria for these myeloproliferative disorders, and these changes are reviewed.]. 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:18300758 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP657425.RAie3M4nGVMj92d8mC5KNDeJVm4f67sydIREspLfG_KWs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:43+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}