@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP527749.RANqYkdJ5EbTd7s1KyNmQsAnmxkX0fvr7DXIAY093zMVg> .
@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:NP527749.RANqYkdJ5EbTd7s1KyNmQsAnmxkX0fvr7DXIAY093zMVg130_head {
  this: np:hasAssertion dgn-np:NP527749.RANqYkdJ5EbTd7s1KyNmQsAnmxkX0fvr7DXIAY093zMVg130_assertion;
    np:hasProvenance dgn-np:NP527749.RANqYkdJ5EbTd7s1KyNmQsAnmxkX0fvr7DXIAY093zMVg130_provenance;
    np:hasPublicationInfo dgn-np:NP527749.RANqYkdJ5EbTd7s1KyNmQsAnmxkX0fvr7DXIAY093zMVg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP527749.RANqYkdJ5EbTd7s1KyNmQsAnmxkX0fvr7DXIAY093zMVg130_assertion a np:Assertion .
  
  dgn-np:NP527749.RANqYkdJ5EbTd7s1KyNmQsAnmxkX0fvr7DXIAY093zMVg130_provenance a np:Provenance .
  
  dgn-np:NP527749.RANqYkdJ5EbTd7s1KyNmQsAnmxkX0fvr7DXIAY093zMVg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP527749.RANqYkdJ5EbTd7s1KyNmQsAnmxkX0fvr7DXIAY093zMVg130_assertion {
  miriam-gene:57126 a ncit:C16612 .
  
  lld:C1292778 a ncit:C7057 .
  
  dgn-gda:DGN87522c14287429307196f863b62b6312 sio:SIO_000628 miriam-gene:57126, lld:C1292778;
    a sio:SIO_001121 .
}

dgn-np:NP527749.RANqYkdJ5EbTd7s1KyNmQsAnmxkX0fvr7DXIAY093zMVg130_provenance {
  dgn-np:NP527749.RANqYkdJ5EbTd7s1KyNmQsAnmxkX0fvr7DXIAY093zMVg130_assertion dcterms:description
      "[Increased PRV-1 mRNA expression and the presence of Jak2(V617F) mutation in peripheral blood granulocytes are specific markers for chronic myeloproliferative disorders (MPD), which facilitate the differential diagnosis between polycythemia vera (PV) and secondary erythrocytosis (SE) and may be helpful for monitoring treatment efficacy in MPD patients.]. 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:17852451;
    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:NP527749.RANqYkdJ5EbTd7s1KyNmQsAnmxkX0fvr7DXIAY093zMVg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:16+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" .
}