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Q40917020-7F5B8FAD-4BFA-4082-B286-40A8239D51EA
Q40917020-7F5B8FAD-4BFA-4082-B286-40A8239D51EA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40917020-7F5B8FAD-4BFA-4082-B286-40A8239D51EA
The Gly571Arg mutation, associated with the autonomic and sensory disorder congenital insensitivity to pain with anhidrosis, causes the inactivation of the NTRK1/nerve growth factor receptor.
P2860
Q40917020-7F5B8FAD-4BFA-4082-B286-40A8239D51EA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40917020-7F5B8FAD-4BFA-4082-B286-40A8239D51EA
rank
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type
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Statement
wasDerivedFrom
f3df453f79d4a2ba71f06af6c9e2d91c945d66e3
P2860
Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type IV)