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Q34467171-20022C4D-8D6B-4C7C-9AE8-EFD17ECE2FE0
Q34467171-20022C4D-8D6B-4C7C-9AE8-EFD17ECE2FE0
BestRank
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http://www.wikidata.org/entity/statement/Q34467171-20022C4D-8D6B-4C7C-9AE8-EFD17ECE2FE0
The Fibroblast Growth Factor signaling pathway
P2860
Q34467171-20022C4D-8D6B-4C7C-9AE8-EFD17ECE2FE0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34467171-20022C4D-8D6B-4C7C-9AE8-EFD17ECE2FE0
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wasDerivedFrom
f7d04e8a3ba5996cc668d03d25dfc51cdca56171
P2860
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.