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:_5 ;
    pav:version "20131211" .
  sub:_4 prov:value "We flanked the entire coding region of Shox2 with LoxP sites (10), such as to induce deletion upon exposure to the Cre recombinase (Fig. 1). Mice carrying such a floxed allele as well as a fully deleted copy and the limb-specific Prx1-Cre transgene (11) (hereafter referred to as Shox2  c/?) were thus devoid of any Shox2 transcript in their developing limbs (Fig. 1 b and c). We looked at Runx2 (mRNA) expression in Shox2  c/- mice, and, strikingly, very few Runx2-positive cells were scored in the humerus at E12.5 (Fig. 5  a)." ;
    prov:wasQuotedFrom pubmed:16537395 .
  sub:_5 rdfs:label "Selventa" .
  sub:assertion prov:hadPrimarySource pubmed:16537395 ;
    prov:wasDerivedFrom beldoc: , sub:_4 .
}