@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo> .
@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:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_head {
  this: np:hasAssertion dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_assertion;
    np:hasProvenance dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_provenance;
    np:hasPublicationInfo dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_assertion a np:Assertion .
  
  dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_provenance a np:Provenance .
  
  dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0040028 a ncit:C7057 .
  
  dgn-gda:DGNb17531b523bee0b79de1b3c97a77a4e3 sio:SIO_000628 miriam-gene:3717, lld:C0040028;
    a sio:SIO_001121 .
}

dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_provenance {
  dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_assertion dcterms:description
      "[The frequency of V617F was 65 percent among patients with polycythemia vera (83 of 128), 57 percent among patients with idiopathic myelofibrosis (13 of 23), and 23 percent among patients with essential thrombocythemia (21 of 93).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:15858187;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:08+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" .
}