sub:provenance {
  beldoc: dce:description "Approximately 61,000 statements." ;
    dce:rights "Copyright (c) 2011-2012, Selventa. All rights reserved." ;
    dce:title "BEL Framework Large Corpus Document" ;
    pav:authoredBy sub:_4 ;
    pav:version "20131211" .
  sub:_3 prov:value "More important as a cause of respiratory chain dysfunction is a de¢ciency of the adenine nucleotide translocator (ANT). This has been described in one child with mitochondrial myopathy, and has been attributed to a speci¢c defect of the muscle/heart subunit ANT1 [25]. The lack of cardiac symptoms in that child at age 8 is a little surprising, because a `knockout' mouse de¢cient in ANT1 showed not only mitochondrial myopathy but also hypertrophic cardiomyopathy with mitochondrial proliferation [26]." ;
    prov:wasQuotedFrom pubmed:9714805 .
  sub:_4 rdfs:label "Selventa" .
  sub:assertion prov:hadPrimarySource pubmed:9714805 ;
    prov:wasDerivedFrom beldoc: , sub:_3 .
}