@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP792071.RAijZMDrBHW4FdAqf8PRurOX6_nxE8qu9Gwu7fPZ0pKFE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP792071.RAijZMDrBHW4FdAqf8PRurOX6_nxE8qu9Gwu7fPZ0pKFE130_head {
  this: np:hasAssertion dgn-np:NP792071.RAijZMDrBHW4FdAqf8PRurOX6_nxE8qu9Gwu7fPZ0pKFE130_assertion;
    np:hasProvenance dgn-np:NP792071.RAijZMDrBHW4FdAqf8PRurOX6_nxE8qu9Gwu7fPZ0pKFE130_provenance;
    np:hasPublicationInfo dgn-np:NP792071.RAijZMDrBHW4FdAqf8PRurOX6_nxE8qu9Gwu7fPZ0pKFE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP792071.RAijZMDrBHW4FdAqf8PRurOX6_nxE8qu9Gwu7fPZ0pKFE130_assertion a np:Assertion .
  
  dgn-np:NP792071.RAijZMDrBHW4FdAqf8PRurOX6_nxE8qu9Gwu7fPZ0pKFE130_provenance a np:Provenance .
  
  dgn-np:NP792071.RAijZMDrBHW4FdAqf8PRurOX6_nxE8qu9Gwu7fPZ0pKFE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP792071.RAijZMDrBHW4FdAqf8PRurOX6_nxE8qu9Gwu7fPZ0pKFE130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0027022 a ncit:C7057 .
  
  dgn-gda:DGN627e0c217f45d0e87c5c90265c15e66e sio:SIO_000628 miriam-gene:3717, lld:C0027022;
    a sio:SIO_001122 .
}

dgn-np:NP792071.RAijZMDrBHW4FdAqf8PRurOX6_nxE8qu9Gwu7fPZ0pKFE130_provenance {
  dgn-np:NP792071.RAijZMDrBHW4FdAqf8PRurOX6_nxE8qu9Gwu7fPZ0pKFE130_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:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP792071.RAijZMDrBHW4FdAqf8PRurOX6_nxE8qu9Gwu7fPZ0pKFE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:44+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}