@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is> .
@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:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_head {
  this: np:hasAssertion dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_assertion;
    np:hasProvenance dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_provenance;
    np:hasPublicationInfo dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_assertion a np:Assertion .
  
  dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_provenance a np:Provenance .
  
  dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0024305 a ncit:C7057 .
  
  dgn-gda:DGNab713066f705c89193c194fa0b42d7b3 sio:SIO_000628 miriam-gene:3717, lld:C0024305;
    a sio:SIO_001121 .
}

dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_provenance {
  dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_assertion dcterms:description
      "[This case may be of interest not only due to the rare coexistence of PMN and NHL, but also because of the undetermined clinical significance of JAK2 mutation in this subset of patients.]. 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:21508404;
    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:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:26+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" .
}