@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_head {
  this: np:hasAssertion dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_assertion;
    np:hasProvenance dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_provenance;
    np:hasPublicationInfo dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_assertion a np:Assertion .
  
  dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_provenance a np:Provenance .
  
  dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0027013 a ncit:C7057 .
  
  dgn-gda:DGN4a841c4c588835b0a2182b1f97867a60 sio:SIO_000628 miriam-gene:3717, lld:C0027013;
    a sio:SIO_001121 .
}

dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_provenance {
  dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_assertion dcterms:description
      "[In the current study, mutation analysis for JAK2(V617F) was performed in peripheral blood mononuclear cells (PBMC) from 157 patients with myelofibrosis with myeloid metaplasia (MMM) including 117 with agnogenic (AMM), 22 with postpolycythaemic (PPMM), and 18 with post-thrombocythaemic (PTMM) myeloid metaplasia.]. 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:16225651;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:35+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}