PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 17108110-2 2006 The disease is caused primarily by a methionine to threonine substitution of residue 918 in the kinase domain of the RET receptor (2B-RET); however, the molecular mechanisms that lead to the disease phenotype are unclear. Methionine 37-47 ret proto-oncogene Homo sapiens 117-120 17108110-2 2006 The disease is caused primarily by a methionine to threonine substitution of residue 918 in the kinase domain of the RET receptor (2B-RET); however, the molecular mechanisms that lead to the disease phenotype are unclear. Methionine 37-47 ret proto-oncogene Homo sapiens 134-137