@dpavot:27129268 JSONTXT

{"project":"PGR-UNK","denotations":[{"id":"T1","span":{"begin":73,"end":78},"obj":"9187"},{"id":"T2","span":{"begin":151,"end":159},"obj":"HP:0001022"},{"id":"T3","span":{"begin":53,"end":58},"obj":"123041"},{"id":"T4","span":{"begin":44,"end":51},"obj":"123041"}],"relations":[{"id":"R1","pred":"unknown","subj":"T2","obj":"T1"},{"id":"R2","pred":"unknown","subj":"T3","obj":"T2"},{"id":"R3","pred":"unknown","subj":"T4","obj":"T2"}],"text":"Recent studies have linked mutations in the SLC24A4 (NCKX4) and SLC24A5 (NCKX5) genes to amylogenesis imperfecta (AI) and non-syndromic oculocutaneous albinism (OCA6), respectively."}