PubMed:12626384 / 0-168 JSONTXT

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    sentences

    {"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":127},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":127},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":127},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease.\nFabry disease is a lysosomal storage dis"}

    GlycoBiology-FMA

    {"project":"GlycoBiology-FMA","denotations":[{"id":"_T1","span":{"begin":85,"end":95},"obj":"FMAID:82780"},{"id":"_T2","span":{"begin":85,"end":95},"obj":"FMAID:196773"},{"id":"_T3","span":{"begin":147,"end":156},"obj":"FMAID:63836"},{"id":"_T4","span":{"begin":147,"end":156},"obj":"FMAID:162299"}],"namespaces":[{"prefix":"FMAID","uri":"http://purl.org/sig/ont/fma/fma"}],"text":"A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease.\nFabry disease is a lysosomal storage dis"}

    GO-BP

    {"project":"GO-BP","denotations":[{"id":"T1","span":{"begin":96,"end":103},"obj":"http://purl.obolibrary.org/obo/GO_0051235"},{"id":"T2","span":{"begin":157,"end":164},"obj":"http://purl.obolibrary.org/obo/GO_0051235"},{"id":"T3","span":{"begin":96,"end":103},"obj":"http://purl.obolibrary.org/obo/GO_0035732"},{"id":"T4","span":{"begin":157,"end":164},"obj":"http://purl.obolibrary.org/obo/GO_0035732"}],"text":"A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease.\nFabry disease is a lysosomal storage dis"}

    GO-CC

    {"project":"GO-CC","denotations":[{"id":"T1","span":{"begin":147,"end":156},"obj":"http://purl.obolibrary.org/obo/GO_0005764"}],"text":"A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease.\nFabry disease is a lysosomal storage dis"}

    EDAM-topics

    {"project":"EDAM-topics","denotations":[{"id":"T1","span":{"begin":18,"end":33},"obj":"http://edamontology.org/topic_0202"},{"id":"T2","span":{"begin":119,"end":126},"obj":"http://edamontology.org/topic_0634"},{"id":"T3","span":{"begin":134,"end":141},"obj":"http://edamontology.org/topic_0634"},{"id":"T4","span":{"begin":147,"end":156},"obj":"http://edamontology.org/topic_0616"}],"text":"A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease.\nFabry disease is a lysosomal storage dis"}

    EDAM-DFO

    {"project":"EDAM-DFO","denotations":[{"id":"T1","span":{"begin":34,"end":44},"obj":"http://edamontology.org/operation_2424"}],"text":"A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease.\nFabry disease is a lysosomal storage dis"}

    DisGeNET5_gene_disease

    {"project":"DisGeNET5_gene_disease","denotations":[{"id":"12626384-1#0#13#diseaseC0002986","span":{"begin":128,"end":141},"obj":"diseaseC0002986"}],"text":"A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease.\nFabry disease is a lysosomal storage dis"}

    DisGeNET

    {"project":"DisGeNET","denotations":[{"id":"T1","span":{"begin":128,"end":141},"obj":"disease:C0002986"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease.\nFabry disease is a lysosomal storage dis"}

    mondo_disease

    {"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":113,"end":126},"obj":"Disease"},{"id":"T2","span":{"begin":128,"end":141},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0010526"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0010526"}],"text":"A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease.\nFabry disease is a lysosomal storage dis"}