@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24> .
@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:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_head {
  this: np:hasAssertion dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_assertion;
    np:hasProvenance dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_provenance;
    np:hasPublicationInfo dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_assertion a np:Assertion .
  
  dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_provenance a np:Provenance .
  
  dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_assertion {
  miriam-gene:83886 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGN0616aa59124f647aabc408a5a39cdab3 sio:SIO_000628 miriam-gene:83886, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_provenance {
  dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_assertion dcterms:description
      "[Genetic analysis of MPN patient cohorts with adequate sample size and clear clinical annotation are needed to understand the importance of these mutations on MPN phenotype, risk of transformation to leukemia, response to therapy, and influence on overall survival.]. 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:23009937;
    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:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:56+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" .
}