@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP643916.RAdcsBQqvw2vH_Ghz7DI9xL_8RYFBhkkHNIX4yPibTMk8> .
@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:NP643916.RAdcsBQqvw2vH_Ghz7DI9xL_8RYFBhkkHNIX4yPibTMk8130_head {
  this: np:hasAssertion dgn-np:NP643916.RAdcsBQqvw2vH_Ghz7DI9xL_8RYFBhkkHNIX4yPibTMk8130_assertion;
    np:hasProvenance dgn-np:NP643916.RAdcsBQqvw2vH_Ghz7DI9xL_8RYFBhkkHNIX4yPibTMk8130_provenance;
    np:hasPublicationInfo dgn-np:NP643916.RAdcsBQqvw2vH_Ghz7DI9xL_8RYFBhkkHNIX4yPibTMk8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP643916.RAdcsBQqvw2vH_Ghz7DI9xL_8RYFBhkkHNIX4yPibTMk8130_assertion a np:Assertion .
  
  dgn-np:NP643916.RAdcsBQqvw2vH_Ghz7DI9xL_8RYFBhkkHNIX4yPibTMk8130_provenance a np:Provenance .
  
  dgn-np:NP643916.RAdcsBQqvw2vH_Ghz7DI9xL_8RYFBhkkHNIX4yPibTMk8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP643916.RAdcsBQqvw2vH_Ghz7DI9xL_8RYFBhkkHNIX4yPibTMk8130_assertion {
  miriam-gene:5428 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN5ae921730a42d38b8b0c06887bac4f5f sio:SIO_000628 miriam-gene:5428, lld:C0030567;
    a sio:SIO_001121 .
}

dgn-np:NP643916.RAdcsBQqvw2vH_Ghz7DI9xL_8RYFBhkkHNIX4yPibTMk8130_provenance {
  dgn-np:NP643916.RAdcsBQqvw2vH_Ghz7DI9xL_8RYFBhkkHNIX4yPibTMk8130_assertion dcterms:description
      "[We found that marked neuronal cell loss was only observed in a few patients with mitochondrial disease and that all these patients had mutations in polymerase gamma (POLG), which leads to the formation of multiple mitochondrial DNA deletions over time, similar to aging and Parkinson's disease.]. 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:23804100;
    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:NP643916.RAdcsBQqvw2vH_Ghz7DI9xL_8RYFBhkkHNIX4yPibTMk8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:28+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" .
}