PubMed:20106987 / 296-495 JSONTXT

Annnotations TAB JSON ListView MergeView

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/20106987","sourcedb":"PubMed","sourceid":"20106987","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/20106987","text":"Although the majority of the recessive UCMD cases have frameshift or nonsense mutations in COL6A1, COL6A2, or COL6A3, recessive structural mutations in the COL6A2 C-globular region are emerging also.","tracks":[{"project":"sentences","denotations":[{"id":"T3","span":{"begin":0,"end":199},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"T3","pred":"source","obj":"sentences"}]},{"project":"mondo_disease","denotations":[{"id":"T6","span":{"begin":39,"end":43},"obj":"Disease"}],"attributes":[{"id":"A6","pred":"mondo_id","subj":"T6","obj":"http://purl.obolibrary.org/obo/MONDO_0000355"},{"subj":"T6","pred":"source","obj":"mondo_disease"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"sentences","color":"#93e2ec","default":true},{"id":"mondo_disease","color":"#ecdb93"}]}]}}