@dpavot:23086420 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/@dpavot/sourceid/23086420","sourcedb":"@dpavot","sourceid":"23086420","source_url":"https://www.ncbi.nlm.nih.gov/pubmed/23086420","text":"Several myotubularins have been genetically linked to human diseases: MTM1 is mutated in the congenital myopathy X-linked centronuclear or myotubular myopathy (XLCNM) and MTMR14 (JUMPY) has been linked to an autosomal form of such disease, while MTMR2 and MTMR13 are mutated in Charcot-Marie-Tooth (CMT) neuropathies.","tracks":[{"project":"PGR-FAL","denotations":[{"id":"T1","span":{"begin":246,"end":251},"obj":"8898"},{"id":"T2","span":{"begin":104,"end":112},"obj":"HP:0003198"},{"id":"T3","span":{"begin":256,"end":262},"obj":"81846"}],"relations":[{"id":"R1","pred":"false","subj":"T1","obj":"T2"},{"id":"R2","pred":"false","subj":"T3","obj":"T2"}],"attributes":[{"subj":"T1","pred":"source","obj":"PGR-FAL"},{"subj":"T2","pred":"source","obj":"PGR-FAL"},{"subj":"T3","pred":"source","obj":"PGR-FAL"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"PGR-FAL","color":"#93c6ec","default":true}]}]}}