Sepsis remains a diagnostic challenge due to its heterogeneous molecular signatures and complex immune responses. In this study, we develop a logical data analysis framework based on Boolean polynomial rings. This method constructs an ideal $\mathcal{I}$ of selection criteria that isolate empty subsets of previously analyzed patient data. This approach enables the derivation of interpretable classification rules based on biomarker profiles. We demonstrate that logical data analysis identifies distinct logical patterns for positive and negative sepsis classification. For instance, elevated levels of GLP-1 and MyD88 are associated with septic states in our dataset, whereas high TRAIL and low MyD88 concentrations may suggest a non-septic condition. Importantly, a new way to integrate expert knowledge to filter out potential overfitting or dataset-specific artifacts is shown. Our findings highlight the utility of logics in generating transparent, biologically plausible rules for a data-based and expert-based understanding of sepsis. Moreover, we show how data analysis can benefit from algebraic structures.