> top > docs > PubMed:18701717 > annotations

PubMed:18701717 JSONTXT

Annnotations TAB JSON ListView MergeView

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1180-1185 gene:7337 denotes UBE3A
T1 1136-1153 disease:C0162635 denotes Angelman syndrome
R1 T0 T1 associated_with UBE3A,Angelman syndrome

BioLarkPubmedHPO

Id Subject Object Predicate Lexical cue
HP:0000707 65-86 HP:0000707 denotes neurological disorder
HP:0002187 110-135 HP:0002187 denotes severe mental retardation
HP:0002275 137-163 HP:0002275 denotes loss of motor coordination
HP:0002360 169-187 HP:0002360 denotes sleep disturbances
T1 65-86 HP:0000707 denotes neurological disorder
T2 110-135 HP:0002187 denotes severe mental retardation
T3 137-163 HP:0002275 denotes loss of motor coordination
T4 169-187 HP:0002360 denotes sleep disturbances
T1 65-86 HP:0000707 denotes neurological disorder
T2 110-135 HP:0002187 denotes severe mental retardation
T3 137-163 HP:0002275 denotes loss of motor coordination
T4 169-187 HP:0002360 denotes sleep disturbances
T1 65-86 HP:0000707 denotes neurological disorder
T2 110-135 HP:0002187 denotes severe mental retardation
T3 137-163 HP:0002275 denotes loss of motor coordination
T4 169-187 HP:0002360 denotes sleep disturbances

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
18701717-12#122#127#gene7337 1663-1668 gene7337 denotes UBE3A
18701717-12#54#71#diseaseC0162635 1595-1612 diseaseC0162635 denotes Angelman syndrome
122#127#gene733754#71#diseaseC0162635 18701717-12#122#127#gene7337 18701717-12#54#71#diseaseC0162635 associated_with UBE3A,Angelman syndrome

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 23-40 DiseaseOrPhenotypicFeature denotes Angelman syndrome 0007113
T2 42-59 DiseaseOrPhenotypicFeature denotes Angelman syndrome 0007113
T3 65-86 DiseaseOrPhenotypicFeature denotes neurological disorder 0005071
T4 117-135 DiseaseOrPhenotypicFeature denotes mental retardation 0001071
T5 169-187 DiseaseOrPhenotypicFeature denotes sleep disturbances 0100081
T6 959-976 DiseaseOrPhenotypicFeature denotes Angelman syndrome 0007113
T7 1136-1153 DiseaseOrPhenotypicFeature denotes Angelman syndrome 0007113
T8 1595-1612 DiseaseOrPhenotypicFeature denotes Angelman syndrome 0007113