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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 53-74 DiseaseOrPhenotypicFeature denotes Prader-Willi syndrome 0008300
T2 79-96 DiseaseOrPhenotypicFeature denotes Angelman syndrome 0007113
T3 277-298 DiseaseOrPhenotypicFeature denotes Prader-Willi syndrome 0008300
T4 300-303 DiseaseOrPhenotypicFeature denotes PWS 0008300
T5 309-326 DiseaseOrPhenotypicFeature denotes Angelman syndrome 0007113
T6 416-419 DiseaseOrPhenotypicFeature denotes PWS 0008300
T7 479-482 DiseaseOrPhenotypicFeature denotes PWS 0008300
T8 688-691 DiseaseOrPhenotypicFeature denotes PWS 0008300
T9 824-827 DiseaseOrPhenotypicFeature denotes PWS 0008300

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 53-74 Modifier:D011218 denotes Prader-Willi syndrome
T2 79-96 Modifier:D017204 denotes Angelman syndrome
T3 277-298 SpecificDisease:D011218 denotes Prader-Willi syndrome
T4 300-303 SpecificDisease:D011218 denotes PWS
T5 309-326 SpecificDisease:D017204 denotes Angelman syndrome
T6 328-330 SpecificDisease:D017204 denotes AS
T7 416-419 SpecificDisease:D011218 denotes PWS
T8 479-482 SpecificDisease:D011218 denotes PWS
T9 688-691 Modifier:D011218 denotes PWS

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T3364 53-74 Modifier denotes Prader-Willi syndrome D011218
T3365 79-96 Modifier denotes Angelman syndrome D017204
T3366 277-298 SpecificDisease denotes Prader-Willi syndrome D011218
T3367 300-303 SpecificDisease denotes PWS D011218
T3368 309-326 SpecificDisease denotes Angelman syndrome D017204
T3369 328-330 SpecificDisease denotes AS D017204
T3370 416-419 SpecificDisease denotes PWS D011218
T3371 479-482 SpecificDisease denotes PWS D011218
T3372 688-691 Modifier denotes PWS D011218

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T3364 53-74 Modifier denotes Prader-Willi syndrome D011218
T3365 79-96 Modifier denotes Angelman syndrome D017204
T3366 277-298 SpecificDisease denotes Prader-Willi syndrome D011218
T3367 300-303 SpecificDisease denotes PWS D011218
T3368 309-326 SpecificDisease denotes Angelman syndrome D017204
T3369 328-330 SpecificDisease denotes AS D017204
T3370 416-419 SpecificDisease denotes PWS D011218
T3371 479-482 SpecificDisease denotes PWS D011218
T3372 688-691 Modifier denotes PWS D011218

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 53-96 CompositeMention denotes Prader-Willi syndrome and Angelman syndrome
T2 277-298 SpecificDisease denotes Prader-Willi syndrome
T3 300-303 SpecificDisease denotes PWS
T4 309-326 SpecificDisease denotes Angelman syndrome
T5 328-330 SpecificDisease denotes AS
T6 416-419 SpecificDisease denotes PWS
T7 479-482 SpecificDisease denotes PWS
T8 688-691 SpecificDisease denotes PWS
T9 824-830 CompositeMention denotes PWS-AS

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 53-74 SpecificDisease denotes Prader-Willi syndrome
T2 79-96 SpecificDisease denotes Angelman syndrome
T3 277-298 SpecificDisease denotes Prader-Willi syndrome
T4 300-303 SpecificDisease denotes PWS
T5 309-326 SpecificDisease denotes Angelman syndrome
T6 328-330 SpecificDisease denotes AS
T7 416-419 SpecificDisease denotes PWS
T8 479-482 SpecificDisease denotes PWS
T9 688-691 SpecificDisease denotes PWS
T10 824-830 CompositeMention denotes PWS-AS

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 53-74 SpecificDisease denotes Prader-Willi syndrome
T2 79-96 SpecificDisease denotes Angelman syndrome
T3 277-304 SpecificDisease denotes Prader-Willi syndrome (PWS)
T4 309-331 SpecificDisease denotes Angelman syndrome (AS)
T5 416-419 Modifier denotes PWS
T6 479-482 Modifier denotes PWS
T7 688-691 Modifier denotes PWS
T8 824-830 Modifier denotes PWS-AS

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 53-74 SpecificDisease denotes Prader-Willi syndrome
T2 79-96 SpecificDisease denotes Angelman syndrome
T3 277-304 SpecificDisease denotes Prader-Willi syndrome (PWS)
T4 309-331 SpecificDisease denotes Angelman syndrome (AS)
T5 416-419 SpecificDisease denotes PWS
T6 479-482 SpecificDisease denotes PWS
T7 688-691 SpecificDisease denotes PWS
T8 824-848 CompositeMention denotes PWS-AS deletion interval