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Q28249477-B349B2CD-659B-41A2-B7F1-6BD9D70DD694
Q28249477-B349B2CD-659B-41A2-B7F1-6BD9D70DD694
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28249477-B349B2CD-659B-41A2-B7F1-6BD9D70DD694
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
P1476
Q28249477-B349B2CD-659B-41A2-B7F1-6BD9D70DD694
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28249477-B349B2CD-659B-41A2-B7F1-6BD9D70DD694
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
023b74a55557668216637279d05b745a9b1e7086
P1476
A mutation in the homeodomain
......
omal dominant craniosynostosis
@en