PubMed:23528641 / 132-289 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/23528641","sourcedb":"PubMed","sourceid":"23528641","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/23528641","text":"Pitt-Hopkins syndrome (PTHS) is a rare neurodevelopmental genetic disorder, remaining under-diagnosed due to similarities with other known genetic syndromes.","tracks":[{"project":"sentences","denotations":[{"id":"TextSentencer_T2","span":{"begin":0,"end":157},"obj":"Sentence"},{"id":"T2","span":{"begin":0,"end":157},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"TextSentencer_T2","pred":"source","obj":"sentences"},{"subj":"T2","pred":"source","obj":"sentences"}]},{"project":"Allie","denotations":[{"id":"SS1_23528641_1_0","span":{"begin":0,"end":21},"obj":"expanded"},{"id":"SS2_23528641_1_0","span":{"begin":23,"end":27},"obj":"abbr"}],"relations":[{"id":"AE1_23528641_1_0","pred":"abbreviatedTo","subj":"SS1_23528641_1_0","obj":"SS2_23528641_1_0"}],"attributes":[{"subj":"SS1_23528641_1_0","pred":"source","obj":"Allie"},{"subj":"SS2_23528641_1_0","pred":"source","obj":"Allie"}]},{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":0,"end":21},"obj":"ORDO:2896"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"attributes":[{"subj":"AB1","pred":"source","obj":"PubCasesORDO"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"sentences","color":"#d993ec","default":true},{"id":"Allie","color":"#93ecbf"},{"id":"PubCasesORDO","color":"#eca593"}]}]}}