@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55635.RARD_4DtpFJiycbIV_Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc> .
@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:NP55635.RARD_4DtpFJiycbIV_Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130_head {
  this: np:hasAssertion dgn-np:NP55635.RARD_4DtpFJiycbIV_Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130_assertion;
    np:hasProvenance dgn-np:NP55635.RARD_4DtpFJiycbIV_Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130_provenance;
    np:hasPublicationInfo dgn-np:NP55635.RARD_4DtpFJiycbIV_Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55635.RARD_4DtpFJiycbIV_Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130_assertion a np:Assertion .
  
  dgn-np:NP55635.RARD_4DtpFJiycbIV_Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130_provenance a np:Provenance .
  
  dgn-np:NP55635.RARD_4DtpFJiycbIV_Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55635.RARD_4DtpFJiycbIV_Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0001815 a ncit:C7057 .
  
  dgn-gda:DGN29dc7ca10b10530bcf64692ed5f97d7e sio:SIO_000628 miriam-gene:3717, lld:C0001815;
    a sio:SIO_001122 .
}

dgn-np:NP55635.RARD_4DtpFJiycbIV_Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130_provenance {
  dgn-np:NP55635.RARD_4DtpFJiycbIV_Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130_assertion dcterms:description
      "[These data indicate that loss of wild-type clones at the progenitor level is a feature of MF (primary MF, post-ET MF, and post-PV MF), presumably due to expansion of the JAK2 V617F clone and that this characteristic is surprisingly independent of JAK2 V617F homozygosity, suggesting that additional genomic lesions may contribute to this unique molecular process that distinguishes MF from ET and PV.]. 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:20888389;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP55635.RARD_4DtpFJiycbIV_Dog7gJ4Hw4-6Y6NtLGgNwXQI8nc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}