@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP191022.RA3kj4O5MPpgPg1KL_ArYh7v7h20bgE0poxJ3XoLLT2XE> .
@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:NP191022.RA3kj4O5MPpgPg1KL_ArYh7v7h20bgE0poxJ3XoLLT2XE130_head {
  this: np:hasAssertion dgn-np:NP191022.RA3kj4O5MPpgPg1KL_ArYh7v7h20bgE0poxJ3XoLLT2XE130_assertion;
    np:hasProvenance dgn-np:NP191022.RA3kj4O5MPpgPg1KL_ArYh7v7h20bgE0poxJ3XoLLT2XE130_provenance;
    np:hasPublicationInfo dgn-np:NP191022.RA3kj4O5MPpgPg1KL_ArYh7v7h20bgE0poxJ3XoLLT2XE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP191022.RA3kj4O5MPpgPg1KL_ArYh7v7h20bgE0poxJ3XoLLT2XE130_assertion a np:Assertion .
  
  dgn-np:NP191022.RA3kj4O5MPpgPg1KL_ArYh7v7h20bgE0poxJ3XoLLT2XE130_provenance a np:Provenance .
  
  dgn-np:NP191022.RA3kj4O5MPpgPg1KL_ArYh7v7h20bgE0poxJ3XoLLT2XE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP191022.RA3kj4O5MPpgPg1KL_ArYh7v7h20bgE0poxJ3XoLLT2XE130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0032461 a ncit:C7057 .
  
  dgn-gda:DGNb5c5ba13bb067d85de2e991f7b9675a3 sio:SIO_000628 miriam-gene:3717, lld:C0032461;
    a sio:SIO_001121 .
}

dgn-np:NP191022.RA3kj4O5MPpgPg1KL_ArYh7v7h20bgE0poxJ3XoLLT2XE130_provenance {
  dgn-np:NP191022.RA3kj4O5MPpgPg1KL_ArYh7v7h20bgE0poxJ3XoLLT2XE130_assertion dcterms:description
      "[Therefore, by necessity, any discussion of PV must take into consideration these companion myeloproliferative disorders, and since erythrocytosis is the single clinical feature that sets PV apart from IMF and ET, it is clear that the presence of the JAK2 V617F mutation cannot by itself establish a diagnosis of PV.]. 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:16210034;
    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:NP191022.RA3kj4O5MPpgPg1KL_ArYh7v7h20bgE0poxJ3XoLLT2XE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:45+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" .
}