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Q36098636-1C53E1D9-6912-40D6-9815-F7074402AFA6
Q36098636-1C53E1D9-6912-40D6-9815-F7074402AFA6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36098636-1C53E1D9-6912-40D6-9815-F7074402AFA6
Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease.
P2860
Q36098636-1C53E1D9-6912-40D6-9815-F7074402AFA6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36098636-1C53E1D9-6912-40D6-9815-F7074402AFA6
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wasDerivedFrom
38101fc0bb20950a0643a85552a3700ff9b47fda
P2860
Rich annotation of DNA sequencing variants by leveraging the Ensembl Variant Effect Predictor with plugins.