@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP519446.RAILNJrBHJOe1GI-Phb6hicU4c1YhRqL7PZ-Lfxym8-l0> .
@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:NP519446.RAILNJrBHJOe1GI-Phb6hicU4c1YhRqL7PZ-Lfxym8-l0130_head {
  this: np:hasAssertion dgn-np:NP519446.RAILNJrBHJOe1GI-Phb6hicU4c1YhRqL7PZ-Lfxym8-l0130_assertion;
    np:hasProvenance dgn-np:NP519446.RAILNJrBHJOe1GI-Phb6hicU4c1YhRqL7PZ-Lfxym8-l0130_provenance;
    np:hasPublicationInfo dgn-np:NP519446.RAILNJrBHJOe1GI-Phb6hicU4c1YhRqL7PZ-Lfxym8-l0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP519446.RAILNJrBHJOe1GI-Phb6hicU4c1YhRqL7PZ-Lfxym8-l0130_assertion a np:Assertion .
  
  dgn-np:NP519446.RAILNJrBHJOe1GI-Phb6hicU4c1YhRqL7PZ-Lfxym8-l0130_provenance a np:Provenance .
  
  dgn-np:NP519446.RAILNJrBHJOe1GI-Phb6hicU4c1YhRqL7PZ-Lfxym8-l0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP519446.RAILNJrBHJOe1GI-Phb6hicU4c1YhRqL7PZ-Lfxym8-l0130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0026987 a ncit:C7057 .
  
  dgn-gda:DGN60c311b6c020102129ac64edbbc7d117 sio:SIO_000628 miriam-gene:3717, lld:C0026987;
    a sio:SIO_001122 .
}

dgn-np:NP519446.RAILNJrBHJOe1GI-Phb6hicU4c1YhRqL7PZ-Lfxym8-l0130_provenance {
  dgn-np:NP519446.RAILNJrBHJOe1GI-Phb6hicU4c1YhRqL7PZ-Lfxym8-l0130_assertion dcterms:description
      "[A missense somatic mutation in JAK2 gene (JAK2 V617F) has recently been reported in chronic myeloproliferative disorders, including polycythemia vera, essential thrombocythemia and myelofibrosis with myeloid metaplasia, strongly suggesting its role in the pathogenesis of myeloid 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:16247455;
    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:NP519446.RAILNJrBHJOe1GI-Phb6hicU4c1YhRqL7PZ-Lfxym8-l0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:40+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" .
}