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Q39216118-FABA70B6-1CED-4A06-B7B6-D8FFB67AC1C4
Q39216118-FABA70B6-1CED-4A06-B7B6-D8FFB67AC1C4
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http://www.wikidata.org/entity/statement/Q39216118-FABA70B6-1CED-4A06-B7B6-D8FFB67AC1C4
Frequent gain and loss of intronic splicing regulatory elements during the evolution of vertebrates.
P2860
Q39216118-FABA70B6-1CED-4A06-B7B6-D8FFB67AC1C4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39216118-FABA70B6-1CED-4A06-B7B6-D8FFB67AC1C4
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wasDerivedFrom
8ad39587b8e2def6fed2e2c71813c8a04ed502c0
P2860
hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome