PubMed:10194428 / 777-792 JSONTXT

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    DisGeNET5_variant_disease

    {"project":"DisGeNET5_variant_disease","denotations":[{"id":"10194428-5#82#97#diseaseC0018995","span":{"begin":0,"end":15},"obj":"diseaseC0018995"},{"id":"10194428-5#82#97#diseaseC3469186","span":{"begin":0,"end":15},"obj":"diseaseC3469186"},{"id":"10194428-5#82#97#diseaseC0018995","span":{"begin":0,"end":15},"obj":"diseaseC0018995"},{"id":"10194428-5#82#97#diseaseC3469186","span":{"begin":0,"end":15},"obj":"diseaseC3469186"},{"id":"10194428-5#82#97#diseaseC0018995","span":{"begin":0,"end":15},"obj":"diseaseC0018995"},{"id":"10194428-5#82#97#diseaseC3469186","span":{"begin":0,"end":15},"obj":"diseaseC3469186"}],"text":"hemochromatosis"}

    NCBIDiseaseCorpus

    {"project":"NCBIDiseaseCorpus","denotations":[{"id":"T9","span":{"begin":0,"end":15},"obj":"SpecificDisease:D006432"}],"text":"hemochromatosis"}