@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP202116.RA6ZUH77FDO1fbEfwe8qktTCmHF90WTofObGJqrNM6Sdc> .
@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:NP202116.RA6ZUH77FDO1fbEfwe8qktTCmHF90WTofObGJqrNM6Sdc130_head {
  this: np:hasAssertion dgn-np:NP202116.RA6ZUH77FDO1fbEfwe8qktTCmHF90WTofObGJqrNM6Sdc130_assertion ;
    np:hasProvenance dgn-np:NP202116.RA6ZUH77FDO1fbEfwe8qktTCmHF90WTofObGJqrNM6Sdc130_provenance ;
    np:hasPublicationInfo dgn-np:NP202116.RA6ZUH77FDO1fbEfwe8qktTCmHF90WTofObGJqrNM6Sdc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP202116.RA6ZUH77FDO1fbEfwe8qktTCmHF90WTofObGJqrNM6Sdc130_assertion a np:Assertion .
  dgn-np:NP202116.RA6ZUH77FDO1fbEfwe8qktTCmHF90WTofObGJqrNM6Sdc130_provenance a np:Provenance .
  dgn-np:NP202116.RA6ZUH77FDO1fbEfwe8qktTCmHF90WTofObGJqrNM6Sdc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP202116.RA6ZUH77FDO1fbEfwe8qktTCmHF90WTofObGJqrNM6Sdc130_assertion {
  miriam-gene:25 a ncit:C16612 .
  lld:C0032463 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP202116.RA6ZUH77FDO1fbEfwe8qktTCmHF90WTofObGJqrNM6Sdc130_provenance {
  dgn-np:NP202116.RA6ZUH77FDO1fbEfwe8qktTCmHF90WTofObGJqrNM6Sdc130_assertion dcterms:description "[Discovery of a constitutively activating point mutation of the Janus kinase 2 (JAK2) receptor-associated tyrosine kinase in patients with polycythemia vera (PV) and other BCR/ABL-negative myeloproliferative disorders prompted many groups around the world to examine diverse subsets of patients with myeloid diseases for the prevalence of the JAK2 V617F mutation and its clinical and pathological associations.]. 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:17194663 ;
    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:NP202116.RA6ZUH77FDO1fbEfwe8qktTCmHF90WTofObGJqrNM6Sdc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:51+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 ;
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}