@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8> .
@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/v3.0.0/void/> .
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_head {
  this: np:hasAssertion dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_assertion ;
    np:hasProvenance dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_provenance ;
    np:hasPublicationInfo dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_assertion a np:Assertion .
  dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_provenance a np:Provenance .
  dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_assertion {
  miriam-gene:171023 a ncit:C16612 .
  lld:C0032463 a ncit:C7057 .
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    a sio:SIO_001122 .
}
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_provenance {
  dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_assertion dcterms:description "[We have studied the mutational status of TET2 (complete coding region), ASXL1 (exon12), IDH1 (R132), IDH2 (R140 and R172), and c-CBL (exons 8 and 9) in 62 MPN patients (52 essential thrombocythemia (ET), five polycythemia vera (PV), and five primary myelofibrosis (PMF)) negative for both JAK2 (V617F and exon 12) and MPL (exon 10) mutations.]. 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:21904853 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:37+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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> ;
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}