PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
34081916-2	2021	(2021) show that a polyglycine-expanded protein, uN2CpolyG, is translated from an expansion of GGC repeats in the 5" UTR of the NOTCH2NLC (Notch homolog 2 N-terminal-like C) gene, defining a new pathological mechanism for neuronal intranuclear inclusion diseases (NIID).	polyglycine	19-30	notch receptor 2	Homo sapiens	128-134	
34694469-0	2021	Upstream open reading frame with NOTCH2NLC GGC expansion generates polyglycine aggregates and disrupts nucleocytoplasmic transport: implications for polyglycine diseases.	polyglycine	67-78	notch receptor 2	Homo sapiens	33-39	
34694469-0	2021	Upstream open reading frame with NOTCH2NLC GGC expansion generates polyglycine aggregates and disrupts nucleocytoplasmic transport: implications for polyglycine diseases.	polyglycine	149-160	notch receptor 2	Homo sapiens	33-39	
35274390-3	2022	In NIID cases with an expansion of GGC repeats in the 5"-untranslated region (5"-UTR) of the Notch 2 N-terminal like C (NOTCH2NLC) gene, these repeats are located in an upstream open reading frame (uN2C) and result in the production of a polyglycine-containing protein called uN2CpolyG.	polyglycine	238-249	notch receptor 2	Homo sapiens	120-129	
33693509-7	2021	Immunofluorescence on OPDM muscle samples and expressing mutant NOTCH2NLC with (GGC)69 repeat expansions in HEK293 cells indicated that mutant NOTCH2NLC-polyGlycine protein might be a major component of intranuclear inclusions, and contribute to toxicity in cultured cells.	polyglycine	153-164	notch receptor 2	Homo sapiens	64-70	
33693509-7	2021	Immunofluorescence on OPDM muscle samples and expressing mutant NOTCH2NLC with (GGC)69 repeat expansions in HEK293 cells indicated that mutant NOTCH2NLC-polyGlycine protein might be a major component of intranuclear inclusions, and contribute to toxicity in cultured cells.	polyglycine	153-164	notch receptor 2	Homo sapiens	143-149