PubMed:10029606 / 1012-1104 JSONTXT

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    PubTator4TogoVar

    {"project":"PubTator4TogoVar","denotations":[{"id":"10029606_2","span":{"begin":75,"end":80},"obj":"ProteinMutation"}],"attributes":[{"id":"10029606_2_ProteinMutation","pred":"proteinmutation","subj":"10029606_2","obj":"rs1800562"}],"text":"One proband (Y199H) with severe and early iron loading coinherited HH as a C282Y homozygote."}

    sentences

    {"project":"sentences","denotations":[{"id":"TextSentencer_T7","span":{"begin":0,"end":92},"obj":"Sentence"},{"id":"T7","span":{"begin":0,"end":92},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"One proband (Y199H) with severe and early iron loading coinherited HH as a C282Y homozygote."}

    DisGeNET5_variant_disease

    {"project":"DisGeNET5_variant_disease","denotations":[{"id":"10029606-6#75#80#geners1800562","span":{"begin":75,"end":80},"obj":"geners1800562"},{"id":"10029606-6#13#18#geners137852310","span":{"begin":13,"end":18},"obj":"geners137852310"},{"id":"10029606-6#67#69#diseaseC0392514","span":{"begin":67,"end":69},"obj":"diseaseC0392514"}],"relations":[{"id":"75#80#geners180056267#69#diseaseC0392514","pred":"associated_with","subj":"10029606-6#75#80#geners1800562","obj":"10029606-6#67#69#diseaseC0392514"},{"id":"13#18#geners13785231067#69#diseaseC0392514","pred":"associated_with","subj":"10029606-6#13#18#geners137852310","obj":"10029606-6#67#69#diseaseC0392514"}],"text":"One proband (Y199H) with severe and early iron loading coinherited HH as a C282Y homozygote."}