@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP527732.RAEgXt4v8sgs_lxTrngoFOsRZ6V1-Vqi8lEVsGRhNM5ng> .
@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:NP527732.RAEgXt4v8sgs_lxTrngoFOsRZ6V1-Vqi8lEVsGRhNM5ng130_head {
  this: np:hasAssertion dgn-np:NP527732.RAEgXt4v8sgs_lxTrngoFOsRZ6V1-Vqi8lEVsGRhNM5ng130_assertion;
    np:hasProvenance dgn-np:NP527732.RAEgXt4v8sgs_lxTrngoFOsRZ6V1-Vqi8lEVsGRhNM5ng130_provenance;
    np:hasPublicationInfo dgn-np:NP527732.RAEgXt4v8sgs_lxTrngoFOsRZ6V1-Vqi8lEVsGRhNM5ng130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP527732.RAEgXt4v8sgs_lxTrngoFOsRZ6V1-Vqi8lEVsGRhNM5ng130_assertion a np:Assertion .
  
  dgn-np:NP527732.RAEgXt4v8sgs_lxTrngoFOsRZ6V1-Vqi8lEVsGRhNM5ng130_provenance a np:Provenance .
  
  dgn-np:NP527732.RAEgXt4v8sgs_lxTrngoFOsRZ6V1-Vqi8lEVsGRhNM5ng130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP527732.RAEgXt4v8sgs_lxTrngoFOsRZ6V1-Vqi8lEVsGRhNM5ng130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0032463 a ncit:C7057 .
  
  dgn-gda:DGN996a73b6d07de6e1541048c8068ef19b sio:SIO_000628 miriam-gene:3717, lld:C0032463;
    a sio:SIO_001121 .
}

dgn-np:NP527732.RAEgXt4v8sgs_lxTrngoFOsRZ6V1-Vqi8lEVsGRhNM5ng130_provenance {
  dgn-np:NP527732.RAEgXt4v8sgs_lxTrngoFOsRZ6V1-Vqi8lEVsGRhNM5ng130_assertion dcterms:description
      "[A recurrent somatic activating mutation in the nonreceptor tyrosine kinase JAK2 (JAK2V617F) occurs in the majority of patients with the myeloproliferative disorders polycythemia vera, essential thrombocythemia, myelofibrosis with myeloid metaplasia, and, less commonly, chronic myelomonocytic leukemia.]. 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:16365288;
    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:NP527732.RAEgXt4v8sgs_lxTrngoFOsRZ6V1-Vqi8lEVsGRhNM5ng130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:44+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" .
}