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Q47708439-5C005809-91C0-4652-B39B-27DE04755FE2
Q47708439-5C005809-91C0-4652-B39B-27DE04755FE2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-5C005809-91C0-4652-B39B-27DE04755FE2
Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
P2093
Q47708439-5C005809-91C0-4652-B39B-27DE04755FE2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-5C005809-91C0-4652-B39B-27DE04755FE2
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
738e298fa5feaaca35d43475fcba1be052fe7717
P1545
3
http://www.w3.org/2001/XMLSchema#string
P2093
N Swapna
http://www.w3.org/2001/XMLSchema#string