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PubMed:17273972 / 778-797 JSONTXT

Annnotations TAB JSON ListView MergeView

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T7 0-19 DiseaseOrPhenotypicFeature denotes Shprintzen syndrome 0008564|0008644|0018923

TEST-DiseaseOrPhenotypicFeature

Id Subject Object Predicate Lexical cue #label
T5 0-19 DiseaseOrPhenotypicFeature denotes Shprintzen syndrome D004062

Test-merged

Id Subject Object Predicate Lexical cue #label
T5 0-19 DiseaseOrPhenotypicFeature denotes Shprintzen syndrome D004062

Test-merged-2

Id Subject Object Predicate Lexical cue #label
T5 0-19 DiseaseOrPhenotypicFeature denotes Shprintzen syndrome D004062

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB2 0-19 ORDO:567 denotes Shprintzen syndrome