@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4> .
@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 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:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_head {
  this: np:hasAssertion dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_assertion;
    np:hasProvenance dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_provenance;
    np:hasPublicationInfo dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_assertion a np:Assertion .
  
  dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_provenance a np:Provenance .
  
  dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0027022 a ncit:C7057 .
  
  dgn-gda:DGNe65fd3dc319f6cfb48b138813bed0273 sio:SIO_000628 miriam-gene:3717, lld:C0027022;
    a sio:SIO_001122 .
}

dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_provenance {
  dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_assertion dct:description
      "[Given that the identical somatic activating mutation in the JAK2 tyrosine kinase gene (JAK2(V617F)) is observed in most individuals with polycythemia vera, essential thrombocythemia and primary myelofibrosis, there likely are additional genetic events that contribute to the pathogenesis of these phenotypically distinct disorders.]. 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:19287384;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_publicationInfo {
  this: dct:created "2014-10-02T12:32:34+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}