@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP297052.RAWiRUTtFjJ7gv4gurVSrMSgqJ41T-bWkG7yqKVgMO_XU> .
@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:NP297052.RAWiRUTtFjJ7gv4gurVSrMSgqJ41T-bWkG7yqKVgMO_XU130_head {
  this: np:hasAssertion dgn-np:NP297052.RAWiRUTtFjJ7gv4gurVSrMSgqJ41T-bWkG7yqKVgMO_XU130_assertion;
    np:hasProvenance dgn-np:NP297052.RAWiRUTtFjJ7gv4gurVSrMSgqJ41T-bWkG7yqKVgMO_XU130_provenance;
    np:hasPublicationInfo dgn-np:NP297052.RAWiRUTtFjJ7gv4gurVSrMSgqJ41T-bWkG7yqKVgMO_XU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP297052.RAWiRUTtFjJ7gv4gurVSrMSgqJ41T-bWkG7yqKVgMO_XU130_assertion a np:Assertion .
  
  dgn-np:NP297052.RAWiRUTtFjJ7gv4gurVSrMSgqJ41T-bWkG7yqKVgMO_XU130_provenance a np:Provenance .
  
  dgn-np:NP297052.RAWiRUTtFjJ7gv4gurVSrMSgqJ41T-bWkG7yqKVgMO_XU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP297052.RAWiRUTtFjJ7gv4gurVSrMSgqJ41T-bWkG7yqKVgMO_XU130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0026987 a ncit:C7057 .
  
  dgn-gda:DGN73876d99a6c190b59e07e0941098fbdd sio:SIO_000628 miriam-gene:3717, lld:C0026987;
    a sio:SIO_001121 .
}

dgn-np:NP297052.RAWiRUTtFjJ7gv4gurVSrMSgqJ41T-bWkG7yqKVgMO_XU130_provenance {
  dgn-np:NP297052.RAWiRUTtFjJ7gv4gurVSrMSgqJ41T-bWkG7yqKVgMO_XU130_assertion dcterms:description
      "[These changes and the resultant clinical research are discussed in this article where we argue that discovery of the JAK2 V617F mutation has signalled the much delayed change in therapeutic paradigm for myelofibrosis and possibly other MPNs from palliation and allowing us to move closer to, but not yet attain, a cure.]. 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:22463737;
    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:NP297052.RAWiRUTtFjJ7gv4gurVSrMSgqJ41T-bWkG7yqKVgMO_XU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:49+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" .
}