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Q53851875-D4F81397-0AEB-4019-AB04-659A84CF494E
Q53851875-D4F81397-0AEB-4019-AB04-659A84CF494E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53851875-D4F81397-0AEB-4019-AB04-659A84CF494E
Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.
P2860
Q53851875-D4F81397-0AEB-4019-AB04-659A84CF494E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53851875-D4F81397-0AEB-4019-AB04-659A84CF494E
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
5c134aadc4ad51e242559930d0c25e2fee109bec
P2860
Post-translational modifications of three members of the human MAP1LC3 family and detection of a novel type of modification for MAP1LC3B