awgldk
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Table
SPARQL
Graphs
1
1
Services
1
1
Assets
0
0
Insights
Schema
BETA
Class frequency
Class hierarchy
Q42335979-B5EA9FC9-1C0C-4017-81B0-E51446F5D2D8
Q42335979-B5EA9FC9-1C0C-4017-81B0-E51446F5D2D8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42335979-B5EA9FC9-1C0C-4017-81B0-E51446F5D2D8
Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G.
P2860
Q42335979-B5EA9FC9-1C0C-4017-81B0-E51446F5D2D8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42335979-B5EA9FC9-1C0C-4017-81B0-E51446F5D2D8
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
b6dab9a7d4f492fbea4caed1d8454c7b754fc978
c219bb56a62d283ee305c4f1455950fa82c64084
P2860
Founder effects in two predominant intronic mutations of UNC13D, c.118-308C>T and c.754-1G>C underlie the unusual predominance of type 3 familial hemophagocytic lymphohistiocytosis (FHL3) in Korea