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Q28236792-8BBF2C16-031F-4A75-A48E-62D6055B4AC2
Q28236792-8BBF2C16-031F-4A75-A48E-62D6055B4AC2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28236792-8BBF2C16-031F-4A75-A48E-62D6055B4AC2
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
P698
Q28236792-8BBF2C16-031F-4A75-A48E-62D6055B4AC2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28236792-8BBF2C16-031F-4A75-A48E-62D6055B4AC2
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
35dd7643dbd58f60c6c4f62286b4a524dfbd5bb3
P698
15731757
http://www.w3.org/2001/XMLSchema#string