PubMed:15958417 / 0-167 JSONTXT

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    sentences

    {"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":107},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":107},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":107},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies.\nThe Large(myd) mouse has a loss-of-function mutation in the"}

    GlycoBiology-GDGDB

    {"project":"GlycoBiology-GDGDB","denotations":[{"id":"_T1","span":{"begin":24,"end":29},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383"}],"text":"Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies.\nThe Large(myd) mouse has a loss-of-function mutation in the"}

    uniprot-human

    {"project":"uniprot-human","denotations":[{"id":"T1","span":{"begin":24,"end":29},"obj":"http://www.uniprot.org/uniprot/Q9UH22"}],"text":"Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies.\nThe Large(myd) mouse has a loss-of-function mutation in the"}

    mondo_disease

    {"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":86,"end":106},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0018282"}],"text":"Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies.\nThe Large(myd) mouse has a loss-of-function mutation in the"}

    NCBITAXON

    {"project":"NCBITAXON","denotations":[{"id":"T1","span":{"begin":123,"end":128},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"10088"},{"id":"A2","pred":"db_id","subj":"T1","obj":"10090"}],"text":"Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies.\nThe Large(myd) mouse has a loss-of-function mutation in the"}