@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP194104.RABpDWRip5bgQQL_2BXbzuEWCVaD9CsXNgN5SsPziDZ08> .
@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:NP194104.RABpDWRip5bgQQL_2BXbzuEWCVaD9CsXNgN5SsPziDZ08130_head {
  this: np:hasAssertion dgn-np:NP194104.RABpDWRip5bgQQL_2BXbzuEWCVaD9CsXNgN5SsPziDZ08130_assertion;
    np:hasProvenance dgn-np:NP194104.RABpDWRip5bgQQL_2BXbzuEWCVaD9CsXNgN5SsPziDZ08130_provenance;
    np:hasPublicationInfo dgn-np:NP194104.RABpDWRip5bgQQL_2BXbzuEWCVaD9CsXNgN5SsPziDZ08130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP194104.RABpDWRip5bgQQL_2BXbzuEWCVaD9CsXNgN5SsPziDZ08130_assertion a np:Assertion .
  
  dgn-np:NP194104.RABpDWRip5bgQQL_2BXbzuEWCVaD9CsXNgN5SsPziDZ08130_provenance a np:Provenance .
  
  dgn-np:NP194104.RABpDWRip5bgQQL_2BXbzuEWCVaD9CsXNgN5SsPziDZ08130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP194104.RABpDWRip5bgQQL_2BXbzuEWCVaD9CsXNgN5SsPziDZ08130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNcac187daa9a686db5939977f8225ddd6 sio:SIO_000628 miriam-gene:3717, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP194104.RABpDWRip5bgQQL_2BXbzuEWCVaD9CsXNgN5SsPziDZ08130_provenance {
  dgn-np:NP194104.RABpDWRip5bgQQL_2BXbzuEWCVaD9CsXNgN5SsPziDZ08130_assertion dcterms:description
      "[Abnormalities of tyrosine kinase proteins are well recognised in myeloid malignancies, mutation in the cytoplasmic tyrosine kinase JAK2 (V617F) is key in the pathogenesis of myeloproliferative neoplasms, and translocations involving ABL key in the development of chronic myeloid leukaemia.]. 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:21722956;
    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:NP194104.RABpDWRip5bgQQL_2BXbzuEWCVaD9CsXNgN5SsPziDZ08130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:47+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" .
}