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d745f4461b9fe67edca2bad0fdd7d61ac110e726
d745f4461b9fe67edca2bad0fdd7d61ac110e726
Reference
http://www.wikidata.org/reference/d745f4461b9fe67edca2bad0fdd7d61ac110e726
Q21499136-2BA8DFEF-4A86-42A5-8D99-7217A32B2314
Q21499136-BC2629ED-7C15-4191-BE50-FDEB7184B8C7
Q21499136-E977A6B1-8EE0-4C38-8037-36DB8D831A33
wasDerivedFrom
d745f4461b9fe67edca2bad0fdd7d61ac110e726
Reference
http://www.wikidata.org/reference/d745f4461b9fe67edca2bad0fdd7d61ac110e726
type
Reference
P1640
Mouse Genome Informatics
P248
UniProt-GOA
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression
P459
IMP
P813
2019-04-08T00:00:00Z
http://www.w3.org/2001/XMLSchema#dateTime
P854
annotations?geneProductId=UniProtKB:Q9Z2D6
P813
b441aa14f32ad7a9e6fe04eb80002b4c