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1
Q30390611-7EC9C3B6-7621-480A-837E-E2BCCA741E22
Q30390611-7EC9C3B6-7621-480A-837E-E2BCCA741E22
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30390611-7EC9C3B6-7621-480A-837E-E2BCCA741E22
Truncating mutations in APP cause a distinct neurological phenotype.
P2093
Q30390611-7EC9C3B6-7621-480A-837E-E2BCCA741E22
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30390611-7EC9C3B6-7621-480A-837E-E2BCCA741E22
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
cf5e55400da6d73de298c077a670dbbc1a61adb3
P1545
6
http://www.w3.org/2001/XMLSchema#string
P2093
UCLA Clinical Genomics Center
http://www.w3.org/2001/XMLSchema#string