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Q28249477-374B8B99-F77D-411C-B2F9-B438EEEDD1EB
Q28249477-374B8B99-F77D-411C-B2F9-B438EEEDD1EB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28249477-374B8B99-F77D-411C-B2F9-B438EEEDD1EB
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
P2093
Q28249477-374B8B99-F77D-411C-B2F9-B438EEEDD1EB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28249477-374B8B99-F77D-411C-B2F9-B438EEEDD1EB
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
023b74a55557668216637279d05b745a9b1e7086
P1545
10
http://www.w3.org/2001/XMLSchema#string
P2093
J B Mulliken
http://www.w3.org/2001/XMLSchema#string