Assertion list
mutation (primary) → HasSubevent
Results from Ascent++: 75
mutation → HasSubevent → cancer 0.63
mutation → HasSubevent → amino acid substitutions 0.57
mutation → HasSubevent → amino acid changes 0.55
mutation → HasSubevent → cancer development 0.53
mutation → HasSubevent → evolution 0.53
mutation → HasSubevent → a premature stop codon 0.51
mutation → HasSubevent → increase 0.51
mutation → HasSubevent → shift 0.50
mutation → HasSubevent → premature stop 0.50
mutation → HasSubevent → genomic instability 0.49
mutation → HasSubevent → truncated protein 0.48
mutation → HasSubevent → altered molecular function 0.45
mutation → HasSubevent → failure 0.41
mutation → HasSubevent → muscle weakness 0.41
mutation → HasSubevent → significant reduction 0.40
mutation → HasSubevent → misfolding 0.40
mutation → HasSubevent → variation 0.39
mutation → HasSubevent → different phenotypes 0.39
mutation → HasSubevent → protein 0.39
mutation → HasSubevent → mutant 0.38
mutation → HasSubevent → neurodegeneration 0.36
mutation → HasSubevent → sickle cell anemia 0.35
mutation → HasSubevent → elongated fruit 0.35
mutation → HasSubevent → mitochondrial dysfunction 0.34
mutation → HasSubevent → short protein 0.33
mutation → HasSubevent → life 0.32
mutation → HasSubevent → a high cell division rate 0.32
mutation → HasSubevent → constitutive activation 0.32
mutation → HasSubevent → truncation 0.32
mutation → HasSubevent → an in-frame deletion 0.31
mutation → HasSubevent → beneficial changes 0.31
mutation → HasSubevent → dramatic increase 0.31
mutation → HasSubevent → enzyme 0.31
mutation → HasSubevent → frame-shifts 0.31
mutation → HasSubevent → male infertility 0.31
mutation → HasSubevent → uncontrolled cell growth 0.30
mutation → HasSubevent → homeotic transformations 0.28
mutation → HasSubevent → the inactivation of mc synthesis 0.28
mutation → HasSubevent → broad-spectrum resistance 0.27
mutation → HasSubevent → the evolution of biodiversity 0.27
mutation → HasSubevent → the loss of tda production 0.27
mutation → HasSubevent → vision loss 0.26
mutation → HasSubevent → a gain of function 0.25
mutation → HasSubevent → an amino acid exchange 0.25
mutation → HasSubevent → block 0.25
mutation → HasSubevent → chromosomal instability 0.25
mutation → HasSubevent → complete loss of activity 0.25
mutation → HasSubevent → gene inactivation 0.25
mutation → HasSubevent → hyper-igm immunodeficiency synd… 0.25
mutation → HasSubevent → overexpression 0.25
mutation → HasSubevent → premature termination 0.25
mutation → HasSubevent → short telomeres 0.25
mutation → HasSubevent → thrombocytopenia 0.25
mutation → HasSubevent → xp 0.25
mutation → HasSubevent → deficiency 0.25
mutation → HasSubevent → the death of motor neurons 0.25
mutation → HasSubevent → case 0.24
mutation → HasSubevent → inability 0.24
mutation → HasSubevent → birth defects 0.22
mutation → HasSubevent → blindness 0.22
mutation → HasSubevent → anemia 0.21
mutation → HasSubevent → insulin resistance 0.19
mutation → HasSubevent → new versions of proteins 0.19
mutation → HasSubevent → aberrant signaling 0.16
mutation → HasSubevent → autoimmune disease 0.16
mutation → HasSubevent → constitutive kinase activation 0.16
mutation → HasSubevent → distinctive facial features 0.16
mutation → HasSubevent → excess production 0.16
mutation → HasSubevent → glaucoma 0.16
mutation → HasSubevent → intestinal polyps 0.16
mutation → HasSubevent → leukaemia 0.16
mutation → HasSubevent → misshapen head 0.16
mutation → HasSubevent → motor neuron degeneration 0.16
mutation → HasSubevent → short stature 0.16
mutation → HasSubevent → the insertion of one nucleotide 0.16