PubMed:16321363 / 0-89 JSONTXT

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    TEST-DiseaseOrPhenotypicFeature

    {"project":"TEST-DiseaseOrPhenotypicFeature","denotations":[{"id":"T1","span":{"begin":0,"end":36},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"D018981"}],"text":"Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation."}

    Test-merged-2

    {"project":"Test-merged-2","denotations":[{"id":"T1","span":{"begin":0,"end":36},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"D018981"}],"text":"Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation."}

    sentences

    {"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":89},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":89},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation."}