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Q47708439-DD11D749-8F3F-406C-8F34-172EB1C3DF62
Q47708439-DD11D749-8F3F-406C-8F34-172EB1C3DF62
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-DD11D749-8F3F-406C-8F34-172EB1C3DF62
Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
P356
Q47708439-DD11D749-8F3F-406C-8F34-172EB1C3DF62
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-DD11D749-8F3F-406C-8F34-172EB1C3DF62
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
738e298fa5feaaca35d43475fcba1be052fe7717
P356
10.12688/F1000RESEARCH.12102.1
http://www.w3.org/2001/XMLSchema#string
P356
F1000RESEARCH.12102.1