@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1246138.RAn4RbFFJSXjsTg7xIdOGCI0k1CWqGKXAi7UAEPwgIrUM> .
@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:NP1246138.RAn4RbFFJSXjsTg7xIdOGCI0k1CWqGKXAi7UAEPwgIrUM130_head {
  this: np:hasAssertion dgn-np:NP1246138.RAn4RbFFJSXjsTg7xIdOGCI0k1CWqGKXAi7UAEPwgIrUM130_assertion;
    np:hasProvenance dgn-np:NP1246138.RAn4RbFFJSXjsTg7xIdOGCI0k1CWqGKXAi7UAEPwgIrUM130_provenance;
    np:hasPublicationInfo dgn-np:NP1246138.RAn4RbFFJSXjsTg7xIdOGCI0k1CWqGKXAi7UAEPwgIrUM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1246138.RAn4RbFFJSXjsTg7xIdOGCI0k1CWqGKXAi7UAEPwgIrUM130_assertion a np:Assertion .
  
  dgn-np:NP1246138.RAn4RbFFJSXjsTg7xIdOGCI0k1CWqGKXAi7UAEPwgIrUM130_provenance a np:Provenance .
  
  dgn-np:NP1246138.RAn4RbFFJSXjsTg7xIdOGCI0k1CWqGKXAi7UAEPwgIrUM130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1246138.RAn4RbFFJSXjsTg7xIdOGCI0k1CWqGKXAi7UAEPwgIrUM130_assertion {
  miriam-gene:613 a ncit:C16612 .
  
  lld:C1292778 a ncit:C7057 .
  
  dgn-gda:DGN50e86201087fffef72b2da860c719cae sio:SIO_000628 miriam-gene:613, lld:C1292778;
    a sio:SIO_001121 .
}

dgn-np:NP1246138.RAn4RbFFJSXjsTg7xIdOGCI0k1CWqGKXAi7UAEPwgIrUM130_provenance {
  dgn-np:NP1246138.RAn4RbFFJSXjsTg7xIdOGCI0k1CWqGKXAi7UAEPwgIrUM130_assertion dcterms:description
      "[The discovery of the JAK2V617F mutation followed by the discovery of other genetic abnormalities allowed important progress in the understanding of the pathogenesis and management of myeloproliferative neoplasms (MPN)s. Classical Breakpoint cluster region-Abelson (BCR-ABL)-negative neoplasms include 3 main disorders: essential thrombocythemia (ET), polycythemia vera (PV), and primary myelofibrosis (PMF).]. 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:25486952;
    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:NP1246138.RAn4RbFFJSXjsTg7xIdOGCI0k1CWqGKXAi7UAEPwgIrUM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:10+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" .
}