@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP156552.RAe415JwmIfgVB2vBbM7xoVFdu6NDaVuuO9YuWi47Zvcw> .
@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:NP156552.RAe415JwmIfgVB2vBbM7xoVFdu6NDaVuuO9YuWi47Zvcw130_head {
  this: np:hasAssertion dgn-np:NP156552.RAe415JwmIfgVB2vBbM7xoVFdu6NDaVuuO9YuWi47Zvcw130_assertion;
    np:hasProvenance dgn-np:NP156552.RAe415JwmIfgVB2vBbM7xoVFdu6NDaVuuO9YuWi47Zvcw130_provenance;
    np:hasPublicationInfo dgn-np:NP156552.RAe415JwmIfgVB2vBbM7xoVFdu6NDaVuuO9YuWi47Zvcw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP156552.RAe415JwmIfgVB2vBbM7xoVFdu6NDaVuuO9YuWi47Zvcw130_assertion a np:Assertion .
  
  dgn-np:NP156552.RAe415JwmIfgVB2vBbM7xoVFdu6NDaVuuO9YuWi47Zvcw130_provenance a np:Provenance .
  
  dgn-np:NP156552.RAe415JwmIfgVB2vBbM7xoVFdu6NDaVuuO9YuWi47Zvcw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP156552.RAe415JwmIfgVB2vBbM7xoVFdu6NDaVuuO9YuWi47Zvcw130_assertion {
  miriam-gene:7066 a ncit:C16612 .
  
  lld:C1292778 a ncit:C7057 .
  
  dgn-gda:DGN51e40cd4c2070308e8b35f47b4bc09e2 sio:SIO_000628 miriam-gene:7066, lld:C1292778;
    a sio:SIO_001121 .
}

dgn-np:NP156552.RAe415JwmIfgVB2vBbM7xoVFdu6NDaVuuO9YuWi47Zvcw130_provenance {
  dgn-np:NP156552.RAe415JwmIfgVB2vBbM7xoVFdu6NDaVuuO9YuWi47Zvcw130_assertion dcterms:description
      "[Acquired mutations in the juxtamembrane region of MPL (W515K or W515L), the receptor for thrombopoietin, have been described in patients with primary myelofibrosis or essential thrombocythemia, which are chronic myeloproliferative disorders.]. 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:18669880;
    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:NP156552.RAe415JwmIfgVB2vBbM7xoVFdu6NDaVuuO9YuWi47Zvcw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:24+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" .
}