PubMed:23528852 / 0-157
Annnotations
{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/23528852","sourcedb":"PubMed","sourceid":"23528852","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/23528852","text":"A case of TUBA1A mutation presenting with lissencephaly and Hirschsprung disease.\nGene mutation of tubulin alpha-1A (TUBA1A), a critical component of microtu","tracks":[{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":81},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":81},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"TextSentencer_T1","pred":"source","obj":"sentences"},{"subj":"T1","pred":"source","obj":"sentences"}]},{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":10,"end":16},"obj":"gene:7846"},{"id":"T1","span":{"begin":42,"end":55},"obj":"disease:C0266463"},{"id":"T2","span":{"begin":10,"end":16},"obj":"gene:7846"},{"id":"T3","span":{"begin":60,"end":80},"obj":"disease:C0019569"},{"id":"T4","span":{"begin":10,"end":16},"obj":"gene:7846"},{"id":"T5","span":{"begin":60,"end":80},"obj":"disease:C2931876"},{"id":"T6","span":{"begin":99,"end":115},"obj":"gene:7846"},{"id":"T8","span":{"begin":117,"end":123},"obj":"gene:7846"},{"id":"T10","span":{"begin":117,"end":123},"obj":"gene:7846"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"},{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"},{"id":"R3","pred":"associated_with","subj":"T4","obj":"T5"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"attributes":[{"subj":"T0","pred":"source","obj":"DisGeNET"},{"subj":"T1","pred":"source","obj":"DisGeNET"},{"subj":"T2","pred":"source","obj":"DisGeNET"},{"subj":"T3","pred":"source","obj":"DisGeNET"},{"subj":"T4","pred":"source","obj":"DisGeNET"},{"subj":"T5","pred":"source","obj":"DisGeNET"},{"subj":"T6","pred":"source","obj":"DisGeNET"},{"subj":"T8","pred":"source","obj":"DisGeNET"},{"subj":"T10","pred":"source","obj":"DisGeNET"}]},{"project":"Allie","denotations":[{"id":"SS1_23528852_1_0","span":{"begin":99,"end":115},"obj":"expanded"},{"id":"SS2_23528852_1_0","span":{"begin":117,"end":123},"obj":"abbr"}],"relations":[{"id":"AE1_23528852_1_0","pred":"abbreviatedTo","subj":"SS1_23528852_1_0","obj":"SS2_23528852_1_0"}],"attributes":[{"subj":"SS1_23528852_1_0","pred":"source","obj":"Allie"},{"subj":"SS2_23528852_1_0","pred":"source","obj":"Allie"}]},{"project":"PubCasesHPO","denotations":[{"id":"TI1","span":{"begin":42,"end":55},"obj":"HP:0001339"}],"attributes":[{"subj":"TI1","pred":"source","obj":"PubCasesHPO"}]},{"project":"PubCasesORDO","denotations":[{"id":"TI1","span":{"begin":60,"end":80},"obj":"ORDO:388"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"attributes":[{"subj":"TI1","pred":"source","obj":"PubCasesORDO"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"sentences","color":"#ec93da","default":true},{"id":"DisGeNET","color":"#93ece4"},{"id":"Allie","color":"#ecca93"},{"id":"PubCasesHPO","color":"#b093ec"},{"id":"PubCasesORDO","color":"#93ec96"}]}]}}