PubMed:10029606 / 254-422 JSONTXT

Annnotations TAB JSON ListView MergeView

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/10029606","sourcedb":"PubMed","sourceid":"10029606","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/10029606","text":"X-linked sideroblastic anemia (XLSA) in four unrelated male probands was caused by missense mutations in the erythroid-specific 5-aminolevulinate synthase gene (ALAS2).","tracks":[{"project":"sentences","denotations":[{"id":"TextSentencer_T2","span":{"begin":0,"end":168},"obj":"Sentence"},{"id":"T2","span":{"begin":0,"end":168},"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":"PubCasesHPO","denotations":[{"id":"AB1","span":{"begin":9,"end":29},"obj":"HP:0001924"}],"attributes":[{"subj":"AB1","pred":"source","obj":"PubCasesHPO"}]},{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":0,"end":29},"obj":"ORDO:75563"},{"id":"AB2","span":{"begin":31,"end":35},"obj":"ORDO:75563"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"attributes":[{"subj":"AB1","pred":"source","obj":"PubCasesORDO"},{"subj":"AB2","pred":"source","obj":"PubCasesORDO"}]},{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":0,"end":8},"obj":"HP_0001417"},{"id":"T2","span":{"begin":9,"end":29},"obj":"HP_0001924"},{"id":"T3","span":{"begin":23,"end":29},"obj":"HP_0001903"}],"attributes":[{"subj":"T1","pred":"source","obj":"PubmedHPO"},{"subj":"T2","pred":"source","obj":"PubmedHPO"},{"subj":"T3","pred":"source","obj":"PubmedHPO"}]},{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":161,"end":166},"obj":"gene:212"},{"id":"T1","span":{"begin":0,"end":29},"obj":"disease:C0221018"},{"id":"T2","span":{"begin":161,"end":166},"obj":"gene:212"},{"id":"T3","span":{"begin":31,"end":35},"obj":"disease:C0221018"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"},{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"}],"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"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"sentences","color":"#93ecad","default":true},{"id":"PubCasesHPO","color":"#ec9393"},{"id":"PubCasesORDO","color":"#93acec"},{"id":"PubmedHPO","color":"#c6ec93"},{"id":"DisGeNET","color":"#ec93e0"}]}]}}