@dpavot:25343988 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/@dpavot/sourceid/25343988","sourcedb":"@dpavot","sourceid":"25343988","source_url":"https://www.ncbi.nlm.nih.gov/pubmed/25343988","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.","tracks":[{"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"}],"attributes":[{"subj":"T1","pred":"source","obj":"PGR-FAL"},{"subj":"T2","pred":"source","obj":"PGR-FAL"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"PGR-FAL","color":"#93eca2","default":true}]}]}}