Autor: |
Grouès, Valentin, Moreno, Carlos Vega, Satagopam, Venkata Pardhasaradhi |
Zdroj: |
Data Science; 20220101, Issue: Preprints p1-3, 3p |
Abstrakt: |
Schubert et al. claimed in previous work that mutations in STX1B are associated with epilepsy. We present here a formalization of that claim, stating that all things of class “STX1B mutation” that are in the context of a thing of class “human” frequently have a relation of type “co-occurs with” to a thing of class “epilepsy” in the same context. |
Databáze: |
Supplemental Index |
Externí odkaz: |
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