@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP494885.RAOVfazny3kFg-fouHCiQVnrdVg435PCMpCcjkKcc9rhU> .
@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:NP494885.RAOVfazny3kFg-fouHCiQVnrdVg435PCMpCcjkKcc9rhU130_head {
  this: np:hasAssertion dgn-np:NP494885.RAOVfazny3kFg-fouHCiQVnrdVg435PCMpCcjkKcc9rhU130_assertion;
    np:hasProvenance dgn-np:NP494885.RAOVfazny3kFg-fouHCiQVnrdVg435PCMpCcjkKcc9rhU130_provenance;
    np:hasPublicationInfo dgn-np:NP494885.RAOVfazny3kFg-fouHCiQVnrdVg435PCMpCcjkKcc9rhU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP494885.RAOVfazny3kFg-fouHCiQVnrdVg435PCMpCcjkKcc9rhU130_assertion a np:Assertion .
  
  dgn-np:NP494885.RAOVfazny3kFg-fouHCiQVnrdVg435PCMpCcjkKcc9rhU130_provenance a np:Provenance .
  
  dgn-np:NP494885.RAOVfazny3kFg-fouHCiQVnrdVg435PCMpCcjkKcc9rhU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP494885.RAOVfazny3kFg-fouHCiQVnrdVg435PCMpCcjkKcc9rhU130_assertion {
  miriam-gene:4358 a ncit:C16612 .
  
  lld:C0162670 a ncit:C7057 .
  
  dgn-gda:DGNaf599d59a241808ab74e95deaeeecf81 sio:SIO_000628 miriam-gene:4358, lld:C0162670;
    a sio:SIO_001121 .
}

dgn-np:NP494885.RAOVfazny3kFg-fouHCiQVnrdVg435PCMpCcjkKcc9rhU130_provenance {
  dgn-np:NP494885.RAOVfazny3kFg-fouHCiQVnrdVg435PCMpCcjkKcc9rhU130_assertion dcterms:description
      "[The most recently described mitochondrial myopathies are due to defects in nuclear DNA, including coenzyme Q10 deficiency and mutations in genes controlling mitochondrial DNA abundance and structure, such as POLG, TK2, 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:17053512;
    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:NP494885.RAOVfazny3kFg-fouHCiQVnrdVg435PCMpCcjkKcc9rhU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:55+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" .
}