Sentence examples for terms were mainly from inspiring English sources
When the Romans finally conquered Gaul and imposed their language, a number of Celtic words came into Latin, but the Celtic terms were mainly concerned with rural life.
Missed terms were mainly due to tokenization issues, poor recognition of formulas, and term conjunctions.
The 40 GO terms were mainly distributed in several categories, including photosynthesis, primary metabolism, secondary metabolism, response to stimulus, cell wall, and ribosome.
Significant GO terms were mainly involved in interleukin-1 binding, interleukin-1 receptor activity, hydrogen antiporter activity, calcium ion binding, solute antiporter activity, plasma membrane, antiporter activity, and cation antiporter activity.
The significant GO terms were mainly involved in positive regulation of macromolecule metabolic process and gene expression, plasma membrane, protein localization, enzyme binding, response to oxidative stress and immune system development.
And the significant GO terms were mainly involved in sensory perception of smell or chemical stimulus, olfactory receptor activity, G-protein coupled receptor protein signaling pathway, cell surface receptor linked signal transduction, and other basic metabolic processes.
First-order terms are mainly considered, but the extensions to higher-order terms, as well as to subharmonic rotations, are straightforward.
The proteins associated to these metabolic-related GO terms are mainly AMPK subunits (PRKAA1 and PRKAA2) and NF-kB.
At the first stage, GO terms are mainly involved in metabolic process and development process for both the breeds.
Significantly enriched GO MF terms are mainly related to ion binding function, while many enriched BP terms are associated to lipid metabolism and transport.
The genes associated with the significantly enriched GO terms are mainly involved in response to stress and DNA/RNA damage (RPB4, RECQ4A, CHD1L, WDR61, and CNOT1), cell death and signal transduction (RASSF5, GEM, RAB14, and CACNA1E), energy and transcription regulation (ATP5A1, COX6B1, CDT1, GTF2A2, SIX1, and GMEB2).
