PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
32002787-1	2020	Mutations in the CDKL5 gene, which encodes a serine/threonine kinase, causes a rare encephalopathy, characterized by early-onset epilepsy and severe intellectual disability, named CDKL5 deficiency disorder (CDD).	cholecystokinin C-terminal flanking peptide	45-51	cyclin dependent kinase like 5	Homo sapiens	17-22