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Q30365318-55475803-1E38-4506-8EE6-144B87E83073
Q30365318-55475803-1E38-4506-8EE6-144B87E83073
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30365318-55475803-1E38-4506-8EE6-144B87E83073
The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing loss.
P2860
Q30365318-55475803-1E38-4506-8EE6-144B87E83073
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30365318-55475803-1E38-4506-8EE6-144B87E83073
rank
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type
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Statement
wasDerivedFrom
1a67c2c419d42625e09936217c0b841122d615fc
P2860
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.