@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c> .
@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:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_head {
  this: np:hasAssertion dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_assertion;
    np:hasProvenance dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_provenance;
    np:hasPublicationInfo dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_assertion a np:Assertion .
  
  dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_provenance a np:Provenance .
  
  dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0027022 a ncit:C7057 .
  
  dgn-gda:DGN051f1e423c629ed003edff1ee9b0e721 sio:SIO_000628 miriam-gene:3717, lld:C0027022;
    a sio:SIO_001122 .
}

dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_provenance {
  dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_assertion dcterms:description
      "[Since variability in the JAK2(V617F) allele burden is partly responsible for the distinct phenotypes seen in the myeloproliferative disorders, the objective of this study was to identify modifiers of the allele burden.]. 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:20133898;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:34+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" .
}