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Q33882393-643F4BB5-DC38-4183-A94B-AAB8E1C35967
Q33882393-643F4BB5-DC38-4183-A94B-AAB8E1C35967
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33882393-643F4BB5-DC38-4183-A94B-AAB8E1C35967
A case of 22q11.2 deletion syndrome with Peters anomaly, congenital glaucoma, and heterozygous mutation in CYP1B1
P2860
Q33882393-643F4BB5-DC38-4183-A94B-AAB8E1C35967
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33882393-643F4BB5-DC38-4183-A94B-AAB8E1C35967
rank
NormalRank
type
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Statement
wasDerivedFrom
c5a81175c9bce96d3a15077d01f8813e749a451d
P2860
The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1.