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PubMed:18632931 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 100-106 gene:6323 denotes Nav1.1
T1 55-83 disease:C0338484 denotes familial hemiplegic migraine
T2 108-113 gene:6323 denotes SCN1A
T3 55-83 disease:C0338484 denotes familial hemiplegic migraine
T4 291-296 gene:6323 denotes SCN1A
T5 254-257 disease:C1832884 denotes FHM
R1 T0 T1 associated_with Nav1.1,familial hemiplegic migraine
R2 T2 T3 associated_with SCN1A,familial hemiplegic migraine
R3 T4 T5 associated_with SCN1A,FHM

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
18632931-3#28#34#geners121918628 559-565 geners121918628 denotes Q1489K
18632931-3#15#18#diseaseC1832884 546-549 diseaseC1832884 denotes FHM
28#34#geners12191862815#18#diseaseC1832884 18632931-3#28#34#geners121918628 18632931-3#15#18#diseaseC1832884 associated_with Q1489K,FHM

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
18632931-0#108#113#gene6323 108-113 gene6323 denotes SCN1A
18632931-0#55#83#diseaseC0338484 55-83 diseaseC0338484 denotes familial hemiplegic migraine
18632931-2#55#60#gene6323 291-296 gene6323 denotes SCN1A
18632931-2#18#21#diseaseC1832884 254-257 diseaseC1832884 denotes FHM
108#113#gene632355#83#diseaseC0338484 18632931-0#108#113#gene6323 18632931-0#55#83#diseaseC0338484 associated_with SCN1A,familial hemiplegic migraine
55#60#gene632318#21#diseaseC1832884 18632931-2#55#60#gene6323 18632931-2#18#21#diseaseC1832884 associated_with SCN1A,FHM

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 55-83 DiseaseOrPhenotypicFeature denotes familial hemiplegic migraine 0000700
T2 128-156 DiseaseOrPhenotypicFeature denotes Familial hemiplegic migraine 0000700
T3 158-161 DiseaseOrPhenotypicFeature denotes FHM 0000700
T4 216-234 DiseaseOrPhenotypicFeature denotes migraine with aura 0005475
T5 254-257 DiseaseOrPhenotypicFeature denotes FHM 0000700
T6 546-549 DiseaseOrPhenotypicFeature denotes FHM 0000700
T7 721-724 DiseaseOrPhenotypicFeature denotes can 0012833
T8 1305-1313 DiseaseOrPhenotypicFeature denotes migraine 0005277
T9 1382-1390 DiseaseOrPhenotypicFeature denotes migraine 0005277
T10 1548-1551 DiseaseOrPhenotypicFeature denotes FHM 0000700
T11 1565-1573 DiseaseOrPhenotypicFeature denotes epilepsy 0005027