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Q28268212-7DBB184C-AF09-49F5-84B4-989828F59A06
Q28268212-7DBB184C-AF09-49F5-84B4-989828F59A06
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28268212-7DBB184C-AF09-49F5-84B4-989828F59A06
Absence of TGFBR2 mutations in patients with spontaneous spinal CSF leaks and intracranial hypotension
P2860
Q28268212-7DBB184C-AF09-49F5-84B4-989828F59A06
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28268212-7DBB184C-AF09-49F5-84B4-989828F59A06
rank
NormalRank
type
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Statement
wasDerivedFrom
25198081fb9df96c7af34442ea4d3030b0a99645
P2860
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2