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Q33804950-655B73D2-BC1E-4534-8318-4467A05A36C8
Q33804950-655B73D2-BC1E-4534-8318-4467A05A36C8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33804950-655B73D2-BC1E-4534-8318-4467A05A36C8
A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.
P2860
Q33804950-655B73D2-BC1E-4534-8318-4467A05A36C8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33804950-655B73D2-BC1E-4534-8318-4467A05A36C8
rank
NormalRank
type
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Statement
wasDerivedFrom
efa3fb32171ef07a91cb72eb7010f9eb0c4cc913
P2860
Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.