PubMed:25533456 / 503-688 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/25533456","sourcedb":"PubMed","sourceid":"25533456","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/25533456","text":"Dominant and recessive mutations are found across the entire clinical spectrum; however, recessive Bethlem myopathy is rare, and our understanding of the molecular pathology is limited.","tracks":[{"project":"sentences","denotations":[{"id":"TextSentencer_T4","span":{"begin":0,"end":185},"obj":"Sentence"},{"id":"T4","span":{"begin":0,"end":185},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"TextSentencer_T4","pred":"source","obj":"sentences"},{"subj":"T4","pred":"source","obj":"sentences"}]},{"project":"PubmedHPO","denotations":[{"id":"T5","span":{"begin":107,"end":115},"obj":"HP_0003198"}],"attributes":[{"subj":"T5","pred":"source","obj":"PubmedHPO"}]},{"project":"PubCasesHPO","denotations":[{"id":"AB4","span":{"begin":109,"end":117},"obj":"HP:0003198"}],"attributes":[{"subj":"AB4","pred":"source","obj":"PubCasesHPO"}]},{"project":"PubCasesORDO","denotations":[{"id":"AB3","span":{"begin":99,"end":115},"obj":"ORDO:610"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"attributes":[{"subj":"AB3","pred":"source","obj":"PubCasesORDO"}]},{"project":"HP-phenotype","denotations":[{"id":"T5","span":{"begin":107,"end":115},"obj":"Phenotype"}],"attributes":[{"id":"A5","pred":"hp_id","subj":"T5","obj":"HP:0003198"},{"subj":"T5","pred":"source","obj":"HP-phenotype"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}]},{"project":"mondo_disease","denotations":[{"id":"T11","span":{"begin":99,"end":115},"obj":"Disease"}],"attributes":[{"id":"A11","pred":"mondo_id","subj":"T11","obj":"http://purl.obolibrary.org/obo/MONDO_0008029"},{"id":"A12","pred":"mondo_id","subj":"T11","obj":"http://purl.obolibrary.org/obo/MONDO_0024530"},{"subj":"T11","pred":"source","obj":"mondo_disease"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"sentences","color":"#ec93e8","default":true},{"id":"PubmedHPO","color":"#93ecd5"},{"id":"PubCasesHPO","color":"#ecbb93"},{"id":"PubCasesORDO","color":"#a193ec"},{"id":"HP-phenotype","color":"#9eec93"},{"id":"mondo_disease","color":"#ec93b8"}]}]}}