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Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T0 0-31 DISEASE denotes Hypophosphatemic osteosclerosis
T1 33-45 DISEASE denotes hyperostosis
T2 51-63 DISEASE denotes enthesopathy
T3 64-74 REG denotes associated
T4 75-79 REG denotes with
T5 97-106 VAR denotes mutations
T6 110-114 GENE denotes DMP1
T7 115-123 REG denotes encoding
T8 124-147 GENE denotes dentin matrix protein 1
T9 124-147 GENE denotes dentin matrix protein 1
T10 152-156 GENE denotes SPP1
T11 157-165 REG denotes encoding
T12 166-177 GENE denotes osteopontin
T13 166-177 GENE denotes osteopontin
T14 197-223 DISEASE denotes SIBLING protein osteopathy
T15 213-223 DISEASE denotes osteopathy
T16 229-237 DISEASE denotes SIBLINGs
T17 261-301 GENE denotes secreted calcium-binding phosphoproteins
T18 306-314 REG denotes comprise
T19 326-372 GENE denotes integrin-binding ligand N-linked glycoproteins
T20 374-397 GENE denotes dentin matrix protein-1
T21 399-403 GENE denotes DMP1
T22 406-431 GENE denotes secreted phosphoprotein-1
T23 433-437 GENE denotes SPP1
T24 451-462 GENE denotes osteopontin
T25 464-467 GENE denotes OPN
T26 470-499 GENE denotes integrin-binding sialoprotein
T27 470-499 GENE denotes integrin-binding sialoprotein
T28 501-505 GENE denotes IBSP
T29 519-536 GENE denotes bone sialoprotein
T30 519-536 GENE denotes bone sialoprotein
T31 538-541 GENE denotes BSP
T32 544-584 GENE denotes matrix extracellular phosphoglycoprotein
T33 544-584 GENE denotes matrix extracellular phosphoglycoprotein
T34 586-590 GENE denotes MEPE
T35 586-590 GENE denotes MEPE
T36 597-623 GENE denotes dentin sialophosphoprotein
T37 597-623 GENE denotes dentin sialophosphoprotein
T38 625-629 GENE denotes DSPP
T39 646-649 REG denotes has
T40 711-716 VAR denotes ASARM
T41 731-745 VAR denotes Ser-x-Glu/pSer
T42 766-780 VAR denotes phosphorylated
T43 781-788 POSREG denotes promote
T44 789-796 INTERACTION denotes binding
T45 815-829 GENE denotes hydroxyapatite
T46 834-844 REG denotes regulation
T47 848-865 MPA denotes biomineralization
T48 892-908 NEGREG denotes loss-of-function
T49 939-945 REG denotes encode
T50 950-958 DISEASE denotes SIBLINGs
T51 976-980 GENE denotes DSPP
T52 981-988 REG denotes causing
T54 997-1026 DISEASE denotes autosomal dominant dysplasias
T53 997-1036 DISEASE denotes autosomal dominant dysplasias of dentin
T55 1049-1065 DISEASE denotes skeletal disease
T56 1071-1075 GENE denotes DMP1
T57 1076-1083 REG denotes causing
T59 1084-1120 DISEASE denotes autosomal recessive hypophosphatemic
T58 1084-1136 DISEASE denotes autosomal recessive hypophosphatemic rickets, type 1
T60 1138-1143 DISEASE denotes ARHR1
T61 1168-1176 REG denotes reported
T62 1182-1198 POSREG denotes gain-of-function
T63 1214-1218 GENE denotes DSPP
T64 1222-1226 GENE denotes DMP1
T65 1235-1246 VAR denotes alterations
T66 1250-1254 GENE denotes SPP1
T67 1256-1260 GENE denotes IBSP
T68 1265-1269 GENE denotes MEPE
T69 1298-1329 DISEASE denotes hypophosphatemic osteosclerosis
T70 1334-1346 DISEASE denotes hyperostosis
T71 1347-1357 REG denotes associated
T72 1363-1381 CPA denotes skeletal deformity
T73 1363-1381 DISEASE denotes skeletal deformity
T74 1383-1396 CPA denotes short stature
T75 1398-1410 DISEASE denotes enthesopathy
T76 1412-1422 CPA denotes tooth loss
T77 1412-1422 DISEASE denotes tooth loss
T78 1428-1432 POSREG denotes high
T79 1445-1450 GENE denotes FGF23
T80 1451-1457 MPA denotes levels
T81 1552-1558 REG denotes shared
T82 1576-1585 VAR denotes mutations
T83 1608-1614 REG denotes encode
T84 1634-1643 VAR denotes stop-gain
T85 1646-1654 VAR denotes nonsense
T86 1657-1661 GENE denotes DMP1
T87 1663-1671 VAR denotes c.556G>T
T88 1674-1683 VAR denotes Glu186Ter
T89 1689-1697 VAR denotes missense
T90 1698-1702 GENE denotes SPP1
T91 1704-1710 VAR denotes c.769C
T92 1715-1724 VAR denotes Leu266Phe
T93 1746-1753 REG denotes carried
T94 1782-1790 VAR denotes variants
T95 1824-1833 REG denotes condition
T96 1834-1853 MPA denotes mineral homeostasis
T97 1866-1871 REG denotes basis
T98 1876-1905 DISEASE denotes autosomal recessive disorders
T99 1907-1914 GENE denotes CYP27B1
T100 1915-1925 REG denotes underlying
T101 1926-1961 DISEASE denotes vitamin D dependent rickets, type 1
T102 1967-1972 GENE denotes ABCC6
T103 1973-1983 REG denotes underlying
T104 1989-2042 DISEASE denotes generalized arterial calcification of infancy, type 2
T105 2010-2034 DISEASE denotes calcification of infancy
T106 2047-2071 DISEASE denotes pseudoxanthoma elasticum
T107 2073-2076 DISEASE denotes PXE
T108 2108-2117 REG denotes contained
T109 2118-2122 POSREG denotes high
T110 2123-2130 MPA denotes amounts
T111 2134-2137 GENE denotes OPN
T112 2134-2137 GENE denotes OPN
T113 2254-2280 DISEASE denotes SIBLING protein osteopathy
T114 2270-2280 DISEASE denotes osteopathy
R0 T0 T3 ThemeOf Hypophosphatemic osteosclerosis,associated
R1 T0 T4 ThemeOf Hypophosphatemic osteosclerosis,with
R10 T5 T3 CauseOf mutations,associated
R100 T72 T78 ThemeOf skeletal deformity,high
R101 T74 T71 ThemeOf short stature,associated
R102 T74 T78 ThemeOf short stature,high
R103 T75 T71 ThemeOf enthesopathy,associated
R104 T75 T78 ThemeOf enthesopathy,high
R105 T75 T80 ThemeOf enthesopathy,levels
R106 T76 T71 ThemeOf tooth loss,associated
R107 T80 T78 ThemeOf levels,high
R108 T80 T71 ThemeOf levels,associated
R109 T82 T81 CauseOf mutations,shared
R11 T7 T5 ThemeOf encoding,mutations
R110 T83 T81 ThemeOf encode,shared
R111 T86 T81 ThemeOf DMP1,shared
R112 T86 T82 ThemeOf DMP1,mutations
R113 T86 T83 ThemeOf DMP1,encode
R114 T86 T84 ThemeOf DMP1,stop-gain
R115 T86 T85 ThemeOf DMP1,nonsense
R116 T86 T87 ThemeOf DMP1,c.556G>T
R117 T86 T88 ThemeOf DMP1,Glu186Ter
R118 T86 T89 ThemeOf DMP1,missense
R119 T86 T91 ThemeOf DMP1,c.769C
R12 T6 T5 ThemeOf DMP1,mutations
R120 T86 T92 ThemeOf DMP1,Leu266Phe
R121 T87 T88 ThemeOf c.556G>T,Glu186Ter
R122 T87 T89 ThemeOf c.556G>T,missense
R123 T91 T89 ThemeOf c.769C,missense
R124 T90 T82 ThemeOf SPP1,mutations
R125 T90 T83 ThemeOf SPP1,encode
R126 T90 T84 ThemeOf SPP1,stop-gain
R127 T90 T85 ThemeOf SPP1,nonsense
R128 T90 T87 ThemeOf SPP1,c.556G>T
R129 T90 T88 ThemeOf SPP1,Glu186Ter
R13 T6 T7 ThemeOf DMP1,encoding
R130 T90 T89 ThemeOf SPP1,missense
R131 T90 T91 ThemeOf SPP1,c.769C
R132 T90 T92 ThemeOf SPP1,Leu266Phe
R133 T91 T92 ThemeOf c.769C,Leu266Phe
R134 T92 T89 ThemeOf Leu266Phe,missense
R135 T94 T95 CauseOf variants,condition
R136 T94 T96 CauseOf variants,mineral homeostasis
R137 T94 T97 CauseOf variants,basis
R138 T94 T100 CauseOf variants,underlying
R139 T94 T103 CauseOf variants,underlying
R14 T6 T11 ThemeOf DMP1,encoding
R140 T96 T93 ThemeOf mineral homeostasis,carried
R141 T96 T95 ThemeOf mineral homeostasis,condition
R142 T96 T97 ThemeOf mineral homeostasis,basis
R143 T99 T94 ThemeOf CYP27B1,variants
R144 T101 T93 ThemeOf "vitamin D dependent rickets, type 1",carried
R145 T101 T95 ThemeOf "vitamin D dependent rickets, type 1",condition
R146 T101 T97 ThemeOf "vitamin D dependent rickets, type 1",basis
R147 T101 T100 ThemeOf "vitamin D dependent rickets, type 1",underlying
R148 T101 T103 ThemeOf "vitamin D dependent rickets, type 1",underlying
R149 T104 T93 ThemeOf "generalized arterial calcification of infancy, type 2",carried
R15 T8 T5 ThemeOf dentin matrix protein 1,mutations
R150 T104 T97 ThemeOf "generalized arterial calcification of infancy, type 2",basis
R151 T104 T100 ThemeOf "generalized arterial calcification of infancy, type 2",underlying
R152 T104 T103 ThemeOf "generalized arterial calcification of infancy, type 2",underlying
R153 T106 T93 ThemeOf pseudoxanthoma elasticum,carried
R154 T106 T95 ThemeOf pseudoxanthoma elasticum,condition
R155 T106 T97 ThemeOf pseudoxanthoma elasticum,basis
R156 T106 T100 ThemeOf pseudoxanthoma elasticum,underlying
R157 T106 T103 ThemeOf pseudoxanthoma elasticum,underlying
R158 T107 T93 ThemeOf PXE,carried
R159 T107 T97 ThemeOf PXE,basis
R16 T8 T7 ThemeOf dentin matrix protein 1,encoding
R160 T107 T100 ThemeOf PXE,underlying
R161 T107 T103 ThemeOf PXE,underlying
R162 T109 T108 ThemeOf high,contained
R163 T110 T108 ThemeOf amounts,contained
R164 T110 T109 ThemeOf amounts,high
R165 T111 T108 ThemeOf OPN,contained
R166 T111 T109 ThemeOf OPN,high
R167 T111 T110 ThemeOf OPN,amounts
R17 T8 T11 ThemeOf dentin matrix protein 1,encoding
R18 T10 T5 ThemeOf SPP1,mutations
R19 T10 T7 ThemeOf SPP1,encoding
R2 T0 T18 ThemeOf Hypophosphatemic osteosclerosis,comprise
R20 T10 T11 ThemeOf SPP1,encoding
R21 T12 T5 ThemeOf osteopontin,mutations
R22 T12 T7 ThemeOf osteopontin,encoding
R23 T12 T11 ThemeOf osteopontin,encoding
R24 T12 T18 ThemeOf osteopontin,comprise
R25 T15 T3 ThemeOf osteopathy,associated
R26 T15 T4 ThemeOf osteopathy,with
R27 T15 T7 ThemeOf osteopathy,encoding
R28 T15 T11 ThemeOf osteopathy,encoding
R29 T15 T18 ThemeOf osteopathy,comprise
R3 T1 T3 ThemeOf hyperostosis,associated
R30 T17 T18 ThemeOf secreted calcium-binding phosphoproteins,comprise
R31 T19 T18 ThemeOf integrin-binding ligand N-linked glycoproteins,comprise
R32 T20 T5 ThemeOf dentin matrix protein-1,mutations
R33 T20 T18 ThemeOf dentin matrix protein-1,comprise
R34 T21 T5 ThemeOf DMP1,mutations
R35 T21 T18 ThemeOf DMP1,comprise
R36 T22 T5 ThemeOf secreted phosphoprotein-1,mutations
R37 T22 T18 ThemeOf secreted phosphoprotein-1,comprise
R38 T23 T5 ThemeOf SPP1,mutations
R39 T23 T18 ThemeOf SPP1,comprise
R4 T1 T4 ThemeOf hyperostosis,with
R40 T24 T5 ThemeOf osteopontin,mutations
R41 T24 T18 ThemeOf osteopontin,comprise
R42 T25 T5 ThemeOf OPN,mutations
R43 T25 T18 ThemeOf OPN,comprise
R44 T26 T5 ThemeOf integrin-binding sialoprotein,mutations
R45 T26 T18 ThemeOf integrin-binding sialoprotein,comprise
R46 T28 T5 ThemeOf IBSP,mutations
R47 T28 T18 ThemeOf IBSP,comprise
R48 T29 T5 ThemeOf bone sialoprotein,mutations
R49 T29 T18 ThemeOf bone sialoprotein,comprise
R5 T2 T3 ThemeOf enthesopathy,associated
R50 T31 T5 ThemeOf BSP,mutations
R51 T31 T18 ThemeOf BSP,comprise
R52 T32 T5 ThemeOf matrix extracellular phosphoglycoprotein,mutations
R53 T32 T18 ThemeOf matrix extracellular phosphoglycoprotein,comprise
R54 T34 T18 ThemeOf MEPE,comprise
R55 T36 T18 ThemeOf dentin sialophosphoprotein,comprise
R56 T38 T18 ThemeOf DSPP,comprise
R57 T40 T39 ThemeOf ASARM,has
R58 T40 T42 ThemeOf ASARM,phosphorylated
R59 T40 T43 CauseOf ASARM,promote
R6 T2 T4 ThemeOf enthesopathy,with
R60 T41 T39 ThemeOf Ser-x-Glu/pSer,has
R61 T41 T42 ThemeOf Ser-x-Glu/pSer,phosphorylated
R62 T41 T43 CauseOf Ser-x-Glu/pSer,promote
R63 T41 T46 CauseOf Ser-x-Glu/pSer,regulation
R64 T42 T43 CauseOf phosphorylated,promote
R65 T42 T46 CauseOf phosphorylated,regulation
R66 T44 T43 ThemeOf binding,promote
R67 T44 T46 ThemeOf binding,regulation
R68 T45 T44 ThemeOf hydroxyapatite,binding
R69 T47 T46 ThemeOf biomineralization,regulation
R7 T5 T2 CauseOf mutations,enthesopathy
R70 T51 T49 ThemeOf DSPP,encode
R71 T53 T49 ThemeOf autosomal dominant dysplasias of dentin,encode
R72 T53 T52 ThemeOf autosomal dominant dysplasias of dentin,causing
R73 T53 T57 ThemeOf autosomal dominant dysplasias of dentin,causing
R74 T55 T49 ThemeOf skeletal disease,encode
R75 T55 T52 ThemeOf skeletal disease,causing
R76 T55 T57 ThemeOf skeletal disease,causing
R77 T58 T49 ThemeOf "autosomal recessive hypophosphatemic rickets, type 1",encode
R78 T58 T52 ThemeOf "autosomal recessive hypophosphatemic rickets, type 1",causing
R79 T58 T57 ThemeOf "autosomal recessive hypophosphatemic rickets, type 1",causing
R8 T2 T18 ThemeOf enthesopathy,comprise
R80 T60 T49 ThemeOf ARHR1,encode
R81 T60 T52 ThemeOf ARHR1,causing
R82 T60 T57 ThemeOf ARHR1,causing
R83 T63 T62 ThemeOf DSPP,gain-of-function
R84 T63 T65 ThemeOf DSPP,alterations
R85 T64 T62 ThemeOf DMP1,gain-of-function
R86 T64 T65 ThemeOf DMP1,alterations
R87 T65 T61 CauseOf alterations,reported
R88 T65 T62 CauseOf alterations,gain-of-function
R89 T66 T62 ThemeOf SPP1,gain-of-function
R9 T5 T4 CauseOf mutations,with
R90 T66 T65 ThemeOf SPP1,alterations
R91 T67 T62 ThemeOf IBSP,gain-of-function
R92 T67 T65 ThemeOf IBSP,alterations
R93 T68 T62 ThemeOf MEPE,gain-of-function
R94 T68 T65 ThemeOf MEPE,alterations
R95 T69 T71 ThemeOf hypophosphatemic osteosclerosis,associated
R96 T69 T78 ThemeOf hypophosphatemic osteosclerosis,high
R97 T70 T71 ThemeOf hyperostosis,associated
R98 T70 T78 ThemeOf hyperostosis,high
R99 T72 T71 ThemeOf skeletal deformity,associated