@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP582591.RArXYCS7ihtDZe7IfPem9qCTFtEm25W870PF2eLCpcEsc> .
@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:NP582591.RArXYCS7ihtDZe7IfPem9qCTFtEm25W870PF2eLCpcEsc130_head {
  this: np:hasAssertion dgn-np:NP582591.RArXYCS7ihtDZe7IfPem9qCTFtEm25W870PF2eLCpcEsc130_assertion;
    np:hasProvenance dgn-np:NP582591.RArXYCS7ihtDZe7IfPem9qCTFtEm25W870PF2eLCpcEsc130_provenance;
    np:hasPublicationInfo dgn-np:NP582591.RArXYCS7ihtDZe7IfPem9qCTFtEm25W870PF2eLCpcEsc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP582591.RArXYCS7ihtDZe7IfPem9qCTFtEm25W870PF2eLCpcEsc130_assertion a np:Assertion .
  
  dgn-np:NP582591.RArXYCS7ihtDZe7IfPem9qCTFtEm25W870PF2eLCpcEsc130_provenance a np:Provenance .
  
  dgn-np:NP582591.RArXYCS7ihtDZe7IfPem9qCTFtEm25W870PF2eLCpcEsc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP582591.RArXYCS7ihtDZe7IfPem9qCTFtEm25W870PF2eLCpcEsc130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0001815 a ncit:C7057 .
  
  dgn-gda:DGN6f19f441b7d02d7a124ab164d6c2501c sio:SIO_000628 miriam-gene:3717, lld:C0001815;
    a sio:SIO_001122 .
}

dgn-np:NP582591.RArXYCS7ihtDZe7IfPem9qCTFtEm25W870PF2eLCpcEsc130_provenance {
  dgn-np:NP582591.RArXYCS7ihtDZe7IfPem9qCTFtEm25W870PF2eLCpcEsc130_assertion dcterms:description
      "[The JAK2(V617F) mutation is present in almost all patients with polycythemia vera (PV), large proportions of patients with essential thrombocythemia and idiopathic myelofibrosis, and less frequently in atypical myeloproliferative disorders (MPD).]. 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:17145859;
    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:NP582591.RArXYCS7ihtDZe7IfPem9qCTFtEm25W870PF2eLCpcEsc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:09+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" .
}