@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP296254.RAD-n6nbmWeruWCIDbrMpJRJFsIkxdUNi5JJA78mJQtFA> .
@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:NP296254.RAD-n6nbmWeruWCIDbrMpJRJFsIkxdUNi5JJA78mJQtFA130_head {
  this: np:hasAssertion dgn-np:NP296254.RAD-n6nbmWeruWCIDbrMpJRJFsIkxdUNi5JJA78mJQtFA130_assertion;
    np:hasProvenance dgn-np:NP296254.RAD-n6nbmWeruWCIDbrMpJRJFsIkxdUNi5JJA78mJQtFA130_provenance;
    np:hasPublicationInfo dgn-np:NP296254.RAD-n6nbmWeruWCIDbrMpJRJFsIkxdUNi5JJA78mJQtFA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP296254.RAD-n6nbmWeruWCIDbrMpJRJFsIkxdUNi5JJA78mJQtFA130_assertion a np:Assertion .
  
  dgn-np:NP296254.RAD-n6nbmWeruWCIDbrMpJRJFsIkxdUNi5JJA78mJQtFA130_provenance a np:Provenance .
  
  dgn-np:NP296254.RAD-n6nbmWeruWCIDbrMpJRJFsIkxdUNi5JJA78mJQtFA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP296254.RAD-n6nbmWeruWCIDbrMpJRJFsIkxdUNi5JJA78mJQtFA130_assertion {
  miriam-gene:11232 a ncit:C16612 .
  
  lld:C0342782 a ncit:C7057 .
  
  dgn-gda:DGNa01402eb8c4c76dcd9db6b31cca856b1 sio:SIO_000628 miriam-gene:11232, lld:C0342782;
    a sio:SIO_001121 .
}

dgn-np:NP296254.RAD-n6nbmWeruWCIDbrMpJRJFsIkxdUNi5JJA78mJQtFA130_provenance {
  dgn-np:NP296254.RAD-n6nbmWeruWCIDbrMpJRJFsIkxdUNi5JJA78mJQtFA130_assertion dcterms:description
      "[Mitochondrial DNA depletion is caused by germline deletions and duplications of segments within the mtDNA as well as germline mutations in the nuclear genes responsible for mtDNA duplication (the polymerase apparatus including POLG, POLG2 and PEO1) and mtDNA maintenance (those genes that regulate the deoxynucleotide triphosphate pools and other functions including TP1, TK2, DGUOK, SUCLA1, SUCLA2, ANT1, RRM2B and MPV17).]. 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:20558295;
    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:NP296254.RAD-n6nbmWeruWCIDbrMpJRJFsIkxdUNi5JJA78mJQtFA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:48+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" .
}