@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk> .
@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:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_head {
  this: np:hasAssertion dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_assertion;
    np:hasProvenance dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_provenance;
    np:hasPublicationInfo dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_assertion a np:Assertion .
  
  dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_provenance a np:Provenance .
  
  dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C1292778 a ncit:C7057 .
  
  dgn-gda:DGN963ee3df7e511a1436a679a2b03cbdda sio:SIO_000628 miriam-gene:3717, lld:C1292778;
    a sio:SIO_001122 .
}

dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_provenance {
  dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_assertion dcterms:description
      "[However, it is very clear that some patients with classical PV lack the JAK2 V617F mutation, while some patients with other chronic myeloproliferative disorders such as idiopathic myelofibrosis (IMF) and essential thrombocytosis (ET) also express the JAK2 V617F mutation.]. 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:16210034;
    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:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:39+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" .
}