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Q34097381-E82C4B3E-5FDD-4B3E-B2BD-31E254FDCCF4
Q34097381-E82C4B3E-5FDD-4B3E-B2BD-31E254FDCCF4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34097381-E82C4B3E-5FDD-4B3E-B2BD-31E254FDCCF4
exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels.
P2860
Q34097381-E82C4B3E-5FDD-4B3E-B2BD-31E254FDCCF4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34097381-E82C4B3E-5FDD-4B3E-B2BD-31E254FDCCF4
rank
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type
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Statement
wasDerivedFrom
7ecff3e8966ca577d6dffcbe2e5d6d9ba0ae3024
P2860
11-cis retinol dehydrogenase mutations as a major cause of the congenital night-blindness disorder known as fundus albipunctatus