PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
27010345-6	2016	Oxime analog 7o displayed the most potent EGFR TK inhibitory activity with an IC50 of 0.07 muM, which was analogous to the positive control.	Oximes	0-5	epidermal growth factor receptor	Homo sapiens	42-46	
34773452-1	2021	A series of 5-(4-pyridyl)-1,2,4-triazoles hybrids with acetophenones and their oxime derivatives was rationally designed and synthesized as epidermal growth factor receptor (EGFR) kinase inhibitors.	Oximes	79-84	epidermal growth factor receptor	Homo sapiens	140-172	
34773452-1	2021	A series of 5-(4-pyridyl)-1,2,4-triazoles hybrids with acetophenones and their oxime derivatives was rationally designed and synthesized as epidermal growth factor receptor (EGFR) kinase inhibitors.	Oximes	79-84	epidermal growth factor receptor	Homo sapiens	174-178