PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
2011576-6	1991	A 20-residue synthetic peptide (termed 2.1) from a non-Ca2(+)-binding, disulfide-rich domain of SPARC also exhibited a dose-dependent inhibition of [3H]thymidine uptake in endothelial cells within 24 hr after release from G0 phase.	Tritium	149-151	secreted protein acidic and cysteine rich	Bos taurus	96-101	
8419407-7	1993	A synthetic peptide from another cationic region of SPARC (peptide 2.3) increased [3H]-thymidine incorporation by BAE cells and fibroblasts in a dose-dependent manner.	Tritium	83-85	secreted protein acidic and cysteine rich	Bos taurus	52-57	
2011576-9	1991	Maximum inhibition of [3H]thymidine uptake by SPARC and peptide 2.1 occurred during the early-to-middle G1 phase of the endothelial-cell cycle.	Tritium	23-25	secreted protein acidic and cysteine rich	Bos taurus	46-51