PubMed:19929939 / 887-1135 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/19929939","sourcedb":"PubMed","sourceid":"19929939","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/19929939","text":"A novel heterozygous mutation in exon 18 of the CYLD gene (c.2449delT) was identified, with a deletion of one nucleotide resulting in a premature translational termination codon at amino acid position 831 on the affected allele (p.Cys817Valfs X15).","tracks":[{"project":"sentences","denotations":[{"id":"TextSentencer_T12","span":{"begin":0,"end":248},"obj":"Sentence"},{"id":"T12","span":{"begin":0,"end":248},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"TextSentencer_T12","pred":"source","obj":"sentences"},{"subj":"T12","pred":"source","obj":"sentences"}]},{"project":"tmVarCorpus","denotations":[{"id":"T1","span":{"begin":59,"end":69},"obj":"DNAMutation:c|DEL|2449|T"},{"id":"T2","span":{"begin":229,"end":246},"obj":"ProteinMutation:p|FS|C|817|V|15"}],"attributes":[{"subj":"T1","pred":"source","obj":"tmVarCorpus"},{"subj":"T2","pred":"source","obj":"tmVarCorpus"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"sentences","color":"#d3ec93","default":true},{"id":"tmVarCorpus","color":"#eb93ec"}]}]}}