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Q42208514-CA733FBF-CA5C-4D89-9728-CD59E2ED3084
Q42208514-CA733FBF-CA5C-4D89-9728-CD59E2ED3084
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42208514-CA733FBF-CA5C-4D89-9728-CD59E2ED3084
PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French study
P2860
Q42208514-CA733FBF-CA5C-4D89-9728-CD59E2ED3084
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42208514-CA733FBF-CA5C-4D89-9728-CD59E2ED3084
rank
NormalRank
type
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wasDerivedFrom
493a335688547941702d1de73ab25f5619af9646
P2860
Interstitial deletion 9q22.32-q33.2 associated with additional familial translocation t(9;17)(q34.11;p11.2) in a patient with Gorlin-Goltz syndrome and features of Nail-Patella syndrome