@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1020194.RAuUALCY-KeWQ-x4VwvnjvHhzQAKUuxW2k7XXJz34xN3E> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1020194.RAuUALCY-KeWQ-x4VwvnjvHhzQAKUuxW2k7XXJz34xN3E130_head {
  this: np:hasAssertion dgn-np:NP1020194.RAuUALCY-KeWQ-x4VwvnjvHhzQAKUuxW2k7XXJz34xN3E130_assertion;
    np:hasProvenance dgn-np:NP1020194.RAuUALCY-KeWQ-x4VwvnjvHhzQAKUuxW2k7XXJz34xN3E130_provenance;
    np:hasPublicationInfo dgn-np:NP1020194.RAuUALCY-KeWQ-x4VwvnjvHhzQAKUuxW2k7XXJz34xN3E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1020194.RAuUALCY-KeWQ-x4VwvnjvHhzQAKUuxW2k7XXJz34xN3E130_assertion a np:Assertion .
  
  dgn-np:NP1020194.RAuUALCY-KeWQ-x4VwvnjvHhzQAKUuxW2k7XXJz34xN3E130_provenance a np:Provenance .
  
  dgn-np:NP1020194.RAuUALCY-KeWQ-x4VwvnjvHhzQAKUuxW2k7XXJz34xN3E130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1020194.RAuUALCY-KeWQ-x4VwvnjvHhzQAKUuxW2k7XXJz34xN3E130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0001815 a ncit:C7057 .
  
  dgn-gda:DGN8a22aa00c4a1aa985f702d457c1778eb sio:SIO_000628 miriam-gene:3717, lld:C0001815;
    a sio:SIO_001122 .
}

dgn-np:NP1020194.RAuUALCY-KeWQ-x4VwvnjvHhzQAKUuxW2k7XXJz34xN3E130_provenance {
  dgn-np:NP1020194.RAuUALCY-KeWQ-x4VwvnjvHhzQAKUuxW2k7XXJz34xN3E130_assertion dcterms:description
      "[Given their diagnostic relevance, it is also beneficial and relatively straightforward to screen JAK2 V617F negative patients for JAK2 exon 12 mutations (in the case of erythrocytosis) or MPL exon 10 mutations (thrombocytosis or myelofibrosis) using appropriate assays.]. 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:23057517;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1020194.RAuUALCY-KeWQ-x4VwvnjvHhzQAKUuxW2k7XXJz34xN3E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:28+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}