> top > docs > PubMed:10023663 > annotations

PubMed:10023663 JSONTXT

Annnotations TAB JSON ListView MergeView

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10023663-2#40#52#geners74799832 350-362 geners74799832 denotes Met918-->Thr
10023663-2#0#5#diseaseC0025269 310-315 diseaseC0025269 denotes MEN2B
40#52#geners747998320#5#diseaseC0025269 10023663-2#40#52#geners74799832 10023663-2#0#5#diseaseC0025269 associated_with Met918-->Thr,MEN2B

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10023663-0#61#64#gene5979 61-64 gene5979 denotes RET
10023663-0#20#35#diseaseC0266292 20-35 diseaseC0266292 denotes renal anomalies
10023663-0#65#70#diseaseC0025269 65-70 diseaseC0025269 denotes MEN2B
10023663-3#23#26#gene5979 424-427 gene5979 denotes RET
10023663-3#62#67#gene5979 463-468 gene5979 denotes MEN2A
10023663-3#121#134#diseaseC0019569 522-535 diseaseC0019569 denotes aganglionosis
10023663-3#136#156#diseaseC0019569 537-557 diseaseC0019569 denotes Hirschsprung disease
10023663-3#121#134#diseaseC0019569 522-535 diseaseC0019569 denotes aganglionosis
10023663-4#39#64#gene1621 599-624 gene1621 denotes dopamine beta-hydroxylase
10023663-4#102#107#diseaseC0025269 662-667 diseaseC0025269 denotes MEN2B
10023663-5#7#10#gene5979 759-762 gene5979 denotes RET
10023663-5#104#119#diseaseC0017075 856-871 diseaseC0017075 denotes ganglioneuromas
10023663-8#25#28#gene27352 1172-1175 gene27352 denotes MAP
10023663-8#66#71#diseaseC0025269 1213-1218 diseaseC0025269 denotes MEN2B
10023663-9#50#53#gene5979 1397-1400 gene5979 denotes RET
10023663-9#102#115#diseaseC0000768 1449-1462 diseaseC0000768 denotes malformations
61#64#gene597920#35#diseaseC0266292 10023663-0#61#64#gene5979 10023663-0#20#35#diseaseC0266292 associated_with RET,renal anomalies
61#64#gene597965#70#diseaseC0025269 10023663-0#61#64#gene5979 10023663-0#65#70#diseaseC0025269 associated_with RET,MEN2B
23#26#gene5979121#134#diseaseC0019569 10023663-3#23#26#gene5979 10023663-3#121#134#diseaseC0019569 associated_with RET,aganglionosis
23#26#gene5979136#156#diseaseC0019569 10023663-3#23#26#gene5979 10023663-3#136#156#diseaseC0019569 associated_with RET,Hirschsprung disease
23#26#gene5979121#134#diseaseC0019569 10023663-3#23#26#gene5979 10023663-3#121#134#diseaseC0019569 associated_with RET,aganglionosis
62#67#gene5979121#134#diseaseC0019569 10023663-3#62#67#gene5979 10023663-3#121#134#diseaseC0019569 associated_with MEN2A,aganglionosis
62#67#gene5979136#156#diseaseC0019569 10023663-3#62#67#gene5979 10023663-3#136#156#diseaseC0019569 associated_with MEN2A,Hirschsprung disease
62#67#gene5979121#134#diseaseC0019569 10023663-3#62#67#gene5979 10023663-3#121#134#diseaseC0019569 associated_with MEN2A,aganglionosis
39#64#gene1621102#107#diseaseC0025269 10023663-4#39#64#gene1621 10023663-4#102#107#diseaseC0025269 associated_with dopamine beta-hydroxylase,MEN2B
7#10#gene5979104#119#diseaseC0017075 10023663-5#7#10#gene5979 10023663-5#104#119#diseaseC0017075 associated_with RET,ganglioneuromas
25#28#gene2735266#71#diseaseC0025269 10023663-8#25#28#gene27352 10023663-8#66#71#diseaseC0025269 associated_with MAP,MEN2B
50#53#gene5979102#115#diseaseC0000768 10023663-9#50#53#gene5979 10023663-9#102#115#diseaseC0000768 associated_with RET,malformations

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 101-120 HP_0100568 denotes endocrine neoplasia
T2 111-120 HP_0002664 denotes neoplasia
T3 143-161 HP_0000006 denotes autosomal dominant
T4 207-234 HP_0002865 denotes medullary thyroid carcinoma
T5 217-234 HP_0002890 denotes thyroid carcinoma
T6 236-253 HP_0002666 denotes pheochromocytomas
T7 293-308 HP_0003005 denotes ganglioneuromas
T8 479-506 HP_0002865 denotes medullary thyroid carcinoma
T9 489-506 HP_0002890 denotes thyroid carcinoma
T10 537-557 HP_0002251 denotes Hirschsprung disease
T11 814-820 HP_0002664 denotes tumors
T12 856-871 HP_0003005 denotes ganglioneuromas
T13 979-988 HP_0002664 denotes neoplasms
T14 1049-1055 HP_0002664 denotes tumors
T15 1443-1462 HP_0012210 denotes renal malformations
T16 1443-1462 HP_0000077 denotes renal malformations

DisGeNET

Id Subject Object Predicate Lexical cue
T0 424-427 gene:5979 denotes RET
T1 522-535 disease:C0019569 denotes aganglionosis
T2 463-468 gene:5979 denotes MEN2A
T3 522-535 disease:C0019569 denotes aganglionosis
T4 1397-1400 gene:5979 denotes RET
T5 1401-1406 disease:C0025269 denotes MEN2B
T6 1397-1400 gene:5979 denotes RET
T7 1449-1462 disease:C0000768 denotes malformations
T8 1530-1533 gene:5979 denotes Ret
T9 1449-1462 disease:C0000768 denotes malformations
R1 T0 T1 associated_with RET,aganglionosis
R2 T2 T3 associated_with MEN2A,aganglionosis
R3 T4 T5 associated_with RET,MEN2B
R4 T6 T7 associated_with RET,malformations
R5 T8 T9 associated_with Ret,malformations