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Q28593334-F8669F56-9C0D-4659-AF0B-53D8DA4CBB00
Q28593334-F8669F56-9C0D-4659-AF0B-53D8DA4CBB00
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28593334-F8669F56-9C0D-4659-AF0B-53D8DA4CBB00
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression
P1476
Q28593334-F8669F56-9C0D-4659-AF0B-53D8DA4CBB00
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28593334-F8669F56-9C0D-4659-AF0B-53D8DA4CBB00
rank
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type
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Statement
wasDerivedFrom
6ca081f93021109a8aa104a5c0fce99f068ece6a
P1476
MeCP2 deficiency in Rett syndr
......
that affects UBE3A expression
@en