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Q34246106-0E8AEDD4-32DB-4258-8FBC-F9C046CAB350
Q34246106-0E8AEDD4-32DB-4258-8FBC-F9C046CAB350
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34246106-0E8AEDD4-32DB-4258-8FBC-F9C046CAB350
Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the f
P2860
Q34246106-0E8AEDD4-32DB-4258-8FBC-F9C046CAB350
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34246106-0E8AEDD4-32DB-4258-8FBC-F9C046CAB350
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
4b49a77dffd00e54831886429c477ba325f51ba5
P2860
Metabolic studies in an unusual case of asymptomatic familial hypobetalipoproteinemia with hypolphalipoproteinemia and fasting chylomicronemia.