@dpavot:25343988 JSONTXT

{"project":"PGR-FAL","denotations":[{"id":"T1","span":{"begin":173,"end":177},"obj":"6911"},{"id":"T2","span":{"begin":103,"end":122},"obj":"HP:0000007"}],"relations":[{"id":"R1","pred":"false","subj":"T2","obj":"T1"}],"text":"In humans, mutations in several genes involved in the Notch pathway are associated with SDV, with both autosomal recessive (MESP2, DLL3, LFNG, HES7) and autosomal dominant (TBX6) inheritance."}