PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
16860562-5	2006	Surprisingly, no reduction in repair capacity was observed in primary human fibroblasts that overexpressed GFP-polyQ, a polypeptide that induces HR23B-positive inclusions in these transfected cells.	polyglutamine	111-116	RAD23 homolog B, nucleotide excision repair protein	Homo sapiens	145-150	
29401586-0	2018	PolyQ-expanded huntingtin and ataxin-3 sequester ubiquitin adaptors hHR23B and UBQLN2 into aggregates via conjugated ubiquitin.	polyglutamine	0-5	RAD23 homolog B, nucleotide excision repair protein	Homo sapiens	68-74	
29401586-3	2018	We found that polyQ-expanded Htt-N552 and Atx-3 sequester endogenous Ub adaptors, human RAD23 homolog B (hHR23B) and ubiquilin (UBQLN)-2, into inclusions.	polyglutamine	14-19	RAD23 homolog B, nucleotide excision repair protein	Homo sapiens	105-111	
29401586-5	2018	Moreover, polyQ-expanded Htt-N552 and Atx-3 reduce the protein level of xeroderma pigmentosum group C (XPC) by sequestration of hHR23B, suggesting that this process may cut down the available quantity of hHR23B and thus affect its normal function in stabilizing XPC.	polyglutamine	10-15	RAD23 homolog B, nucleotide excision repair protein	Homo sapiens	128-134	
29401586-5	2018	Moreover, polyQ-expanded Htt-N552 and Atx-3 reduce the protein level of xeroderma pigmentosum group C (XPC) by sequestration of hHR23B, suggesting that this process may cut down the available quantity of hHR23B and thus affect its normal function in stabilizing XPC.	polyglutamine	10-15	RAD23 homolog B, nucleotide excision repair protein	Homo sapiens	204-210	
29401586-8	2018	PolyQ-expanded huntingtin and ataxin-3 sequester ubiquitin adaptors hHR23B and UBQLN2 into aggregates via conjugated ubiquitin.	polyglutamine	0-5	RAD23 homolog B, nucleotide excision repair protein	Homo sapiens	68-74