@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP812396.RAgK2v_byOT3-H_81agFycUxvRZuTD1bo4hmFkecGenq8> .
@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:NP812396.RAgK2v_byOT3-H_81agFycUxvRZuTD1bo4hmFkecGenq8130_head {
  this: np:hasAssertion dgn-np:NP812396.RAgK2v_byOT3-H_81agFycUxvRZuTD1bo4hmFkecGenq8130_assertion;
    np:hasProvenance dgn-np:NP812396.RAgK2v_byOT3-H_81agFycUxvRZuTD1bo4hmFkecGenq8130_provenance;
    np:hasPublicationInfo dgn-np:NP812396.RAgK2v_byOT3-H_81agFycUxvRZuTD1bo4hmFkecGenq8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP812396.RAgK2v_byOT3-H_81agFycUxvRZuTD1bo4hmFkecGenq8130_assertion a np:Assertion .
  
  dgn-np:NP812396.RAgK2v_byOT3-H_81agFycUxvRZuTD1bo4hmFkecGenq8130_provenance a np:Provenance .
  
  dgn-np:NP812396.RAgK2v_byOT3-H_81agFycUxvRZuTD1bo4hmFkecGenq8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP812396.RAgK2v_byOT3-H_81agFycUxvRZuTD1bo4hmFkecGenq8130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0014800 a ncit:C7057 .
  
  dgn-gda:DGNa3f41ceb7d59a048ba332a8e4b607bb5 sio:SIO_000628 miriam-gene:3717, lld:C0014800;
    a sio:SIO_001122 .
}

dgn-np:NP812396.RAgK2v_byOT3-H_81agFycUxvRZuTD1bo4hmFkecGenq8130_provenance {
  dgn-np:NP812396.RAgK2v_byOT3-H_81agFycUxvRZuTD1bo4hmFkecGenq8130_assertion dcterms:description
      "[Clinically suspected PV with low serum erythropoietin and absent JAK2(V617F), together with the bone marrow findings of erythroid hyperplasia and subtle megakaryocytic atypia, should prompt an evaluation for an exon 12 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:20472853;
    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:NP812396.RAgK2v_byOT3-H_81agFycUxvRZuTD1bo4hmFkecGenq8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:53+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" .
}