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Q36497317-5A445CDC-4FE1-4576-B57D-1694C8EBB125
Q36497317-5A445CDC-4FE1-4576-B57D-1694C8EBB125
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36497317-5A445CDC-4FE1-4576-B57D-1694C8EBB125
Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012.
P2860
Q36497317-5A445CDC-4FE1-4576-B57D-1694C8EBB125
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36497317-5A445CDC-4FE1-4576-B57D-1694C8EBB125
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
9d3e37ddb9bc26a8f93c589fe78a610db471c584
P2860
Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome.