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PubMed:3578281 / 0-45 JSONTXT

Annnotations TAB JSON ListView MergeView

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 0-16 DiseaseClass:D017496 denotes Hypopigmentation
T2 24-45 SpecificDisease:D011218 denotes Prader-Willi syndrome

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T4671 0-16 DiseaseClass denotes Hypopigmentation D017496
T4672 24-45 SpecificDisease denotes Prader-Willi syndrome D011218

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T4671 0-16 DiseaseClass denotes Hypopigmentation D017496
T4672 24-45 SpecificDisease denotes Prader-Willi syndrome D011218

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 24-45 SpecificDisease denotes Prader-Willi syndrome

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 24-45 SpecificDisease denotes Prader-Willi syndrome

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 0-16 DiseaseClass denotes Hypopigmentation
T2 24-45 SpecificDisease denotes Prader-Willi syndrome

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 0-45 CompositeMention denotes Hypopigmentation in the Prader-Willi syndrome