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Q46918278-1BA37F74-2E3B-4904-A4AF-A207D6C94483
Q46918278-1BA37F74-2E3B-4904-A4AF-A207D6C94483
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46918278-1BA37F74-2E3B-4904-A4AF-A207D6C94483
Hyperekplexia: a rare differential of neonatal fits described in a developing country.
P2860
Q46918278-1BA37F74-2E3B-4904-A4AF-A207D6C94483
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46918278-1BA37F74-2E3B-4904-A4AF-A207D6C94483
rank
NormalRank
type
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Statement
wasDerivedFrom
4270a0f2f9161eaaff09bc61f7a832b955e73be8
P2860
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor