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Q24534967-62AD6620-AF26-44BF-A9CB-F285C13F8B58
Q24534967-62AD6620-AF26-44BF-A9CB-F285C13F8B58
BestRank
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http://www.wikidata.org/entity/statement/Q24534967-62AD6620-AF26-44BF-A9CB-F285C13F8B58
Loss of Smad3-mediated negative regulation of Runx2 activity leads to an alteration in cell fate determination
P2860
Q24534967-62AD6620-AF26-44BF-A9CB-F285C13F8B58
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24534967-62AD6620-AF26-44BF-A9CB-F285C13F8B58
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wasDerivedFrom
e849efe9b8e398ab9e986dd88b5d48f92d60924c
P2860
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification