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DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10024460-0#151#160#gene5554 151-160 gene5554 denotes protein-C
10024460-0#151#160#gene5555 151-160 gene5555 denotes protein-C
10024460-0#151#160#gene5554 151-160 gene5554 denotes protein-C
10024460-0#151#160#gene5555 151-160 gene5555 denotes protein-C
10024460-0#39#75#diseaseC0949658 39-75 diseaseC0949658 denotes familial hypertrophic cardiomyopathy
10024460-0#77#80#diseaseC0745103 77-80 diseaseC0745103 denotes FHC
151#160#gene555439#75#diseaseC0949658 10024460-0#151#160#gene5554 10024460-0#39#75#diseaseC0949658 associated_with protein-C,familial hypertrophic cardiomyopathy
151#160#gene555477#80#diseaseC0745103 10024460-0#151#160#gene5554 10024460-0#77#80#diseaseC0745103 associated_with protein-C,FHC
151#160#gene555539#75#diseaseC0949658 10024460-0#151#160#gene5555 10024460-0#39#75#diseaseC0949658 associated_with protein-C,familial hypertrophic cardiomyopathy
151#160#gene555577#80#diseaseC0745103 10024460-0#151#160#gene5555 10024460-0#77#80#diseaseC0745103 associated_with protein-C,FHC
151#160#gene555439#75#diseaseC0949658 10024460-0#151#160#gene5554 10024460-0#39#75#diseaseC0949658 associated_with protein-C,familial hypertrophic cardiomyopathy
151#160#gene555477#80#diseaseC0745103 10024460-0#151#160#gene5554 10024460-0#77#80#diseaseC0745103 associated_with protein-C,FHC
151#160#gene555539#75#diseaseC0949658 10024460-0#151#160#gene5555 10024460-0#39#75#diseaseC0949658 associated_with protein-C,familial hypertrophic cardiomyopathy
151#160#gene555577#80#diseaseC0745103 10024460-0#151#160#gene5555 10024460-0#77#80#diseaseC0745103 associated_with protein-C,FHC

bionlp-st-gro-2013-development

Id Subject Object Predicate Lexical cue
T2 13-27 Protein denotes beta-myosin S2
T7 115-132 ProteinDomain denotes regulatory domain
T8 136-160 Protein denotes myosin-binding protein-C
T9 166-172 Protein denotes myosin
T10 195-201 Tissue denotes muscle
T11 232-255 Protein denotes myosin-binding proteins
T12 257-261 Protein denotes MyBP
T13 264-270 Protein denotes MyBP-C
T14 275-281 Protein denotes MyBP-H
T15 297-305 Protein denotes proteins
T16 327-341 Protein denotes immunoglobulin
T17 369-376 ProteinDomain denotes domains
T18 403-420 ProteinDomain denotes N-terminal domain
T19 424-431 Tissue denotes cardiac
T20 432-438 Protein denotes MyBP-C
T21 444-456 ProteinDomain denotes MyBP-C motif
T26 584-594 ProteinDomain denotes C terminus
T29 647-657 Protein denotes myosin rod
T31 679-690 ProteinDomain denotes this domain
T32 737-743 Protein denotes MyBP-C
T33 759-771 ProteinDomain denotes MyBP-C motif
T35 788-805 CellComponent denotes sarcomeric A-band
T36 809-823 Cell denotes cardiomyocytes
T37 837-847 CellComponent denotes myofibrils
T39 913-925 ProteinDomain denotes MyBP-C motif
T40 990-1000 Protein denotes myosin rod
T42 1039-1050 Protein denotes beta-myosin
T46 1181-1195 Protein denotes beta-myosin S2
T47 1197-1202 MutantProtein denotes R870H
T48 1207-1212 MutantProtein denotes E924K
T50 1233-1239 Protein denotes MyBP-C
T53 1446-1452 Protein denotes myosin
T54 1497-1503 Protein denotes MyBP-C
T57 1540-1542 Protein denotes S2
T59 1566-1580 Protein denotes beta-myosin S2
T62 1623-1629 Protein denotes MyBP-C
T28 611-639 ProteinSubunit denotes the light meromyosin portion
T34 867-876 CellComponent denotes sarcomere
T63 900-904 BindingSiteOfProtein denotes site
T64 1280-1285 MutantProtein denotes R870H
T65 1379-1384 MutantProtein denotes E924K
E1 0-9 Mutation denotes Mutations
E2 39-75 Disease denotes familial hypertrophic cardiomyopathy
E3 77-80 Disease denotes FHC
E4 82-89 NegativeRegulation denotes abolish
E5 94-105 BindingOfProteinToProteinBindingSiteOfProtein denotes interaction
E6 478-493 Phosphorylation denotes phosphorylation
E7 508-516 RegulatoryProcess denotes regulate
E8 517-528 OrganismalProcess denotes contraction
E9 534-549 Phosphorylation denotes phosphorylation
E10 602-607 BindingOfProteinToProteinBindingSiteOfProtein denotes binds
E11 663-675 BindingOfProtein denotes interactions
E13 1026-1035 Mutation denotes mutations
E14 1071-1074 Disease denotes FHC
E15 1164-1167 Disease denotes FHC
E16 1168-1177 Mutation denotes mutations
E17 1226-1232 NegativeRegulation denotes reduce
E18 1240-1247 Binding denotes binding
E19 1393-1402 Mutation denotes mutations
E20 1507-1515 RegulatoryProcess denotes mediated
E21 1523-1534 BindingToProtein denotes interaction
E22 1553-1562 Mutation denotes mutations
E23 1592-1600 Affecting denotes altering
E24 1605-1617 BindingToProtein denotes interactions
E12 892-899 BindingOfProteinToProteinBindingSiteOfProtein denotes binding
E25 1226-1232 NegativeRegulation denotes reduce
R1 T8 T7 hasPart myosin-binding protein-C,regulatory domain
R2 T9 T10 locatedIn myosin,muscle
R3 T15 T17 hasPart proteins,domains
R4 T20 T19 locatedIn MyBP-C,cardiac
R5 T20 T18 hasPart MyBP-C,N-terminal domain
R7 T32 T33 hasPart MyBP-C,MyBP-C motif
R6 T29 T28 hasPart myosin rod,the light meromyosin portion
R9 T33 T35 locatedIn MyBP-C motif,sarcomeric A-band
R10 T35 T36 locatedIn sarcomeric A-band,cardiomyocytes
R11 T33 T37 locatedIn MyBP-C motif,myofibrils
R8 T40 T63 hasPart myosin rod,site
R10 T2 E1 hasPatient beta-myosin S2,Mutations
R11 E1 E2 hasAgent Mutations,familial hypertrophic cardiomyopathy
R12 E1 E4 hasAgent Mutations,abolish
R13 E5 E4 hasPatient interaction,abolish
R14 T2 E5 hasAgent beta-myosin S2,interaction
R15 T7 E5 hasPatient regulatory domain,interaction
R16 T21 E6 hasPatient MyBP-C motif,phosphorylation
R17 E9 E7 hasAgent phosphorylation,regulate
R18 E8 E7 hasPatient contraction,regulate
R19 T26 E10 hasAgent C terminus,binds
R20 T28 E10 hasPatient the light meromyosin portion,binds
R21 T31 E11 hasAgent this domain,interactions
R22 T42 E13 hasPatient beta-myosin,mutations
R23 T46 E16 hasPatient beta-myosin S2,mutations
R24 T47 E17 hasAgent R870H,reduce
R25 E18 E17 hasPatient binding,reduce
R26 T50 E18 hasPatient MyBP-C,binding
R27 E21 E20 hasAgent interaction,mediated
R28 T54 E20 hasPatient MyBP-C,mediated
R29 T54 E21 hasPatient MyBP-C,interaction
R30 T57 E21 hasPatient S2,interaction
R31 T59 E22 hasPatient beta-myosin S2,mutations
R32 E22 E23 hasAgent mutations,altering
R33 E24 E23 hasPatient interactions,altering
R34 T62 E24 hasPatient MyBP-C,interactions
R35 T39 E12 hasAgent MyBP-C motif,binding
R36 T63 E12 hasPatient site,binding
R37 T48 E25 hasAgent E924K,reduce
R38 E18 E25 hasPatient binding,reduce

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 517-528 HP_0001371 denotes contraction

DisGeNET

Id Subject Object Predicate Lexical cue
T0 151-160 gene:5555 denotes protein-C
T1 39-75 disease:C0949658 denotes familial hypertrophic cardiomyopathy
T2 151-160 gene:5554 denotes protein-C
T3 39-75 disease:C0949658 denotes familial hypertrophic cardiomyopathy
T4 151-160 gene:5555 denotes protein-C
T5 77-80 disease:C0745103 denotes FHC
T6 151-160 gene:5554 denotes protein-C
T7 77-80 disease:C0745103 denotes FHC
R1 T0 T1 associated_with protein-C,familial hypertrophic cardiomyopathy
R2 T2 T3 associated_with protein-C,familial hypertrophic cardiomyopathy
R3 T4 T5 associated_with protein-C,FHC
R4 T6 T7 associated_with protein-C,FHC