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Q24644487-8EE19AA8-F5A8-46BB-B2C5-DC60D1525FA3
Q24644487-8EE19AA8-F5A8-46BB-B2C5-DC60D1525FA3
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http://www.wikidata.org/entity/statement/Q24644487-8EE19AA8-F5A8-46BB-B2C5-DC60D1525FA3
Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus)
P2860
Q24644487-8EE19AA8-F5A8-46BB-B2C5-DC60D1525FA3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24644487-8EE19AA8-F5A8-46BB-B2C5-DC60D1525FA3
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wasDerivedFrom
df4728fb21a5e2c84fd071e7231916185cd6d09d
P2860
A missense mutation in the gene for melanocyte-stimulating hormone receptor (MC1R) is associated with the chestnut coat color in horses