@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP261713.RAGLuyJ9LME34jwZMU6nIFawP0_F7pwSNAq7IC4pMfyJg> .
@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:NP261713.RAGLuyJ9LME34jwZMU6nIFawP0_F7pwSNAq7IC4pMfyJg130_head {
  this: np:hasAssertion dgn-np:NP261713.RAGLuyJ9LME34jwZMU6nIFawP0_F7pwSNAq7IC4pMfyJg130_assertion;
    np:hasProvenance dgn-np:NP261713.RAGLuyJ9LME34jwZMU6nIFawP0_F7pwSNAq7IC4pMfyJg130_provenance;
    np:hasPublicationInfo dgn-np:NP261713.RAGLuyJ9LME34jwZMU6nIFawP0_F7pwSNAq7IC4pMfyJg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP261713.RAGLuyJ9LME34jwZMU6nIFawP0_F7pwSNAq7IC4pMfyJg130_assertion a np:Assertion .
  
  dgn-np:NP261713.RAGLuyJ9LME34jwZMU6nIFawP0_F7pwSNAq7IC4pMfyJg130_provenance a np:Provenance .
  
  dgn-np:NP261713.RAGLuyJ9LME34jwZMU6nIFawP0_F7pwSNAq7IC4pMfyJg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP261713.RAGLuyJ9LME34jwZMU6nIFawP0_F7pwSNAq7IC4pMfyJg130_assertion {
  miriam-gene:25 a ncit:C16612 .
  
  lld:C0040028 a ncit:C7057 .
  
  dgn-gda:DGNade94409e07b682002f3d34c381d4b75 sio:SIO_000628 miriam-gene:25, lld:C0040028;
    a sio:SIO_001121 .
}

dgn-np:NP261713.RAGLuyJ9LME34jwZMU6nIFawP0_F7pwSNAq7IC4pMfyJg130_provenance {
  dgn-np:NP261713.RAGLuyJ9LME34jwZMU6nIFawP0_F7pwSNAq7IC4pMfyJg130_assertion dcterms:description
      "[The diagnosis and management of the BCR-ABL-negative myeloproliferative disorders (MPDs) of polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF) are at an explosive crossroads of scientific investigation and evolving paradigms since the discovery of the tyrosine kinase-activating JAK2V617F mutation in 2005.]. 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:18024651;
    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:NP261713.RAGLuyJ9LME34jwZMU6nIFawP0_F7pwSNAq7IC4pMfyJg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}