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Q47708439-3DB4DD73-D5D9-459B-A6DC-3FCC121BF60A
Q47708439-3DB4DD73-D5D9-459B-A6DC-3FCC121BF60A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-3DB4DD73-D5D9-459B-A6DC-3FCC121BF60A
Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
P932
Q47708439-3DB4DD73-D5D9-459B-A6DC-3FCC121BF60A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-3DB4DD73-D5D9-459B-A6DC-3FCC121BF60A
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
738e298fa5feaaca35d43475fcba1be052fe7717
P932
5770997
http://www.w3.org/2001/XMLSchema#string