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A. Formalization of the SylloBio-NLI Resource Generation Process
B. Formalization of Tasks 1 and 2
C. Dictionary of gene and pathway membership
D. Domain-specific pipeline for creating NL instances and E Accessing LLMs
H. Prompting LLMs - Zero-shot prompts
I. Prompting LLMs - Few-shot prompts
J. Results: Misaligned Instruction-Response
K. Results: Ambiguous Impact of Distractors on Reasoning
L. Results: Models Prioritize Contextual Knowledge Over Background Knowledge
M Supplementary Figures and N Supplementary Tables
prompt = Suppose you are a specialist with existing knowledge about a signaling and metabolic molecules and their relations organized into biological pathways and processes. Given premises marked with the letter P and the following number and the conclusion marked with the letter C, determine whether the conclusion logically follows from these premises. If the conclusion logically follows from the premises, you need to return ’True’. If the conclusion does not follow logically from the premises, you need to return ’False’. The output should be a single word <True> or <False>.
"P1: " + Premise 1
"P2: " + Premise 2
"C:" + Conclusion
prompt = Suppose you are a specialist with existing knowledge about a signaling and metabolic molecules and their relations organized into biological pathways and processes. Given premises marked with the letter P and the following number and the conclusion marked with the letter C, determine whether the conclusion logically follows from these premises. If the conclusion logically follows from the premises, you need to return ’True’. If the conclusion does not follow logically from the premises, you need to return ’False’. Specify the premises you used to determine whether the conclusion logically follows from the premises, and only these premises. The output should be a single word <True> or <False>and the numbers of the selected premises after the decimal point, like <True, P1, P2>.
"P1: " + Premise 1
"P2: " + Premise 2
"C:" + Conclusion
Authors:
(1) Magdalena Wysocka, National Biomarker Centre, CRUK-MI, Univ. of Manchester, United Kingdom;
(2) Danilo S. Carvalho, National Biomarker Centre, CRUK-MI, Univ. of Manchester, United Kingdom and Department of Computer Science, Univ. of Manchester, United Kingdom;
(3) Oskar Wysocki, National Biomarker Centre, CRUK-MI, Univ. of Manchester, United Kingdom and ited Kingdom 3 I;
(4) Marco Valentino, Idiap Research Institute, Switzerland;
(5) André Freitas, National Biomarker Centre, CRUK-MI, Univ. of Manchester, United Kingdom, Department of Computer Science, Univ. of Manchester, United Kingdom and Idiap Research Institute, Switzerland.
This paper is available on arxiv under CC BY-NC-SA 4.0 license.