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PubMed:10417280 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 44-62 DiseaseOrPhenotypicFeature denotes Angelman syndromes 0007113
T2 157-178 DiseaseOrPhenotypicFeature denotes Prader-Willi syndrome 0008300
T3 180-183 DiseaseOrPhenotypicFeature denotes PWS 0008300
T4 189-206 DiseaseOrPhenotypicFeature denotes Angelman syndrome 0007113
T5 1157-1160 DiseaseOrPhenotypicFeature denotes PWS 0008300

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 225-250 HP_0000708 denotes neurobehavioral disorders
T2 917-927 HP_0009609 denotes duplicated
T3 1036-1048 HP_0009609 denotes duplications

BioLarkPubmedHPO

Id Subject Object Predicate Lexical cue
HP:0000708 225-250 HP:0000708 denotes neurobehavioral disorders
HP:0000707 225-250 HP:0000707 denotes neurobehavioral disorders
T1 225-250 HP:0000708 denotes neurobehavioral disorders
T2 225-250 HP:0000707 denotes neurobehavioral disorders
T1 225-250 HP:0000708 denotes neurobehavioral disorders
T2 225-250 HP:0000707 denotes neurobehavioral disorders
T1 225-250 HP:0000708 denotes neurobehavioral disorders
T2 225-250 HP:0000707 denotes neurobehavioral disorders

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 27-62 CompositeMention:D011218|D017204 denotes Prader-Willi and Angelman syndromes
T2 157-178 SpecificDisease:D011218 denotes Prader-Willi syndrome
T3 180-183 SpecificDisease:D011218 denotes PWS
T4 189-206 SpecificDisease:D017204 denotes Angelman syndrome
T5 208-210 SpecificDisease:D017204 denotes AS
T6 225-250 DiseaseClass:D019954 denotes neurobehavioral disorders
T7 1157-1160 Modifier:D011218 denotes PWS
T8 1161-1163 Modifier:D017204 denotes AS

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T4925 27-62 CompositeMention denotes Prader-Willi and Angelman syndromes D011218|D017204
T4926 157-178 SpecificDisease denotes Prader-Willi syndrome D011218
T4927 180-183 SpecificDisease denotes PWS D011218
T4928 189-206 SpecificDisease denotes Angelman syndrome D017204
T4929 208-210 SpecificDisease denotes AS D017204
T4930 225-250 DiseaseClass denotes neurobehavioral disorders D019954
T4931 1157-1160 Modifier denotes PWS D011218
T4932 1161-1163 Modifier denotes AS D017204

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T4925 27-62 CompositeMention denotes Prader-Willi and Angelman syndromes D011218|D017204
T4926 157-178 SpecificDisease denotes Prader-Willi syndrome D011218
T4927 180-183 SpecificDisease denotes PWS D011218
T4928 189-206 SpecificDisease denotes Angelman syndrome D017204
T4929 208-210 SpecificDisease denotes AS D017204
T4930 225-250 DiseaseClass denotes neurobehavioral disorders D019954
T4931 1157-1160 Modifier denotes PWS D011218
T4932 1161-1163 Modifier denotes AS D017204

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 27-178 SpecificDisease denotes Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints. Prader-Willi syndrome
T2 189-206 SpecificDisease denotes Angelman syndrome
T3 157-178 SpecificDisease denotes Prader-Willi syndrome
T4 180-183 SpecificDisease denotes PWS
T5 189-206 SpecificDisease denotes Angelman syndrome
T6 208-210 SpecificDisease denotes AS
T7 1157-1160 CompositeMention denotes PWS
T8 1161-1163 CompositeMention denotes AS

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 27-62 CompositeMention denotes Prader-Willi and Angelman syndromes
T2 157-178 SpecificDisease denotes Prader-Willi syndrome
T3 180-183 SpecificDisease denotes PWS
T4 189-206 SpecificDisease denotes Angelman syndrome
T5 208-210 SpecificDisease denotes AS
T6 1157-1163 CompositeMention denotes PWS/AS

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 27-39 DiseaseClass denotes Prader-Willi
T2 44-62 DiseaseClass denotes Angelman syndromes
T3 157-178 SpecificDisease denotes Prader-Willi syndrome
T4 189-206 SpecificDisease denotes Angelman syndrome

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 27-62 CompositeMention denotes Prader-Willi and Angelman syndromes
T2 157-184 SpecificDisease denotes Prader-Willi syndrome (PWS)
T3 189-211 SpecificDisease denotes Angelman syndrome (AS)
T4 1157-1172 CompositeMention denotes PWS/AS patients