PubMed:19025767 / 839-841 JSONTXT

Annnotations TAB JSON ListView MergeView

    PMID_GLOBAL

    {"project":"PMID_GLOBAL","denotations":[{"id":"T16","span":{"begin":0,"end":2},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A16","pred":"mondo_id","subj":"T16","obj":"0008199"},{"id":"A17","pred":"mondo_id","subj":"T16","obj":"0015873"},{"id":"A18","pred":"mondo_id","subj":"T16","obj":"0005180"}],"text":"PD"}

    DisGeNET5_variant_disease

    {"project":"DisGeNET5_variant_disease","denotations":[{"id":"19025767-5#156#158#diseaseC0030567","span":{"begin":0,"end":2},"obj":"diseaseC0030567"}],"text":"PD"}