@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g> .
@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:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_head {
  this: np:hasAssertion dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_assertion;
    np:hasProvenance dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_provenance;
    np:hasPublicationInfo dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_assertion a np:Assertion .
  
  dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_provenance a np:Provenance .
  
  dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0026987 a ncit:C7057 .
  
  dgn-gda:DGNc125252f960315174de6b0db1833d820 sio:SIO_000628 miriam-gene:3717, lld:C0026987;
    a sio:SIO_001121 .
}

dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_provenance {
  dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_assertion dcterms:description
      "[Comparisons of JAK2 mutational status to clonality of hematopoiesis in essential thrombocythemia on the one hand, and to activation of transcription factors in myelofibrosis with myeloid metaplasia on the other hand, suggest that JAK2 mutation could be a second genetic event in a subset of patients.]. 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:16901656;
    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:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:00+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" .
}