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split_0_train_2200
split_0_train_2200
[ { "id": "split_0_train_2200_passage", "type": "progene_text", "text": [ "We have recently identified a gene ( the WFIKKN gene ) on human chromosome 16 ( 16p13.3 ) that encodes a secreted protein containing WAP - type , Follistatin / Kazal type , Kunitz - type and NTR - type protease - inhibitory modules and an Immunoglobulin domain [ Trexler et al. , Proc. Natl. Acad. Sci. USA 98 ( 2001 ) , 3705 - 3709 ] ." ], "offsets": [ [ 0, 336 ] ] } ]
[ { "id": "split_0_train_3233_entity", "type": "progene_text", "text": [ "WFIKKN" ], "offsets": [ [ 41, 47 ] ], "normalized": [] }, { "id": "split_0_train_3234_entity", "type": "progene_text", "text": [ "WAP - type , Follistatin / Kazal type , Kunitz - type and NTR - type protease" ], "offsets": [ [ 133, 210 ] ], "normalized": [] }, { "id": "split_0_train_3235_entity", "type": "progene_text", "text": [ "Immunoglobulin" ], "offsets": [ [ 239, 253 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2201
split_0_train_2201
[ { "id": "split_0_train_2201_passage", "type": "progene_text", "text": [ "In the present work we show that a gene on chromosome 17 encodes a WFIKKN - related protein ( WFIKKNRP ) that has the same domain organization as the WFIKKN protein ." ], "offsets": [ [ 0, 166 ] ] } ]
[ { "id": "split_0_train_3236_entity", "type": "progene_text", "text": [ "WFIKKN - related protein" ], "offsets": [ [ 67, 91 ] ], "normalized": [] }, { "id": "split_0_train_3237_entity", "type": "progene_text", "text": [ "WFIKKNRP" ], "offsets": [ [ 94, 102 ] ], "normalized": [] }, { "id": "split_0_train_3238_entity", "type": "progene_text", "text": [ "WFIKKN" ], "offsets": [ [ 150, 156 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2202
split_0_train_2202
[ { "id": "split_0_train_2202_passage", "type": "progene_text", "text": [ "The exon - intron structure of the two genes is also similar as both genes have a single phase 0 intron that splits their WAP domains in equivalent positions ." ], "offsets": [ [ 0, 159 ] ] } ]
[]
[]
[]
[]
split_0_train_2203
split_0_train_2203
[ { "id": "split_0_train_2203_passage", "type": "progene_text", "text": [ "In view of the presence of several protease inhibitory modules in these proteins it seems likely that they serve to control the action of multiple types of proteases ." ], "offsets": [ [ 0, 167 ] ] } ]
[ { "id": "split_0_train_3239_entity", "type": "progene_text", "text": [ "protease" ], "offsets": [ [ 35, 43 ] ], "normalized": [] }, { "id": "split_0_train_3240_entity", "type": "progene_text", "text": [ "proteases" ], "offsets": [ [ 156, 165 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2204
split_0_train_2204
[ { "id": "split_0_train_2204_passage", "type": "progene_text", "text": [ "The tissue expression pattern of the two proteins , however , is markedly different suggesting that they have distinct biological roles ." ], "offsets": [ [ 0, 137 ] ] } ]
[]
[]
[]
[]
split_0_train_2205
split_0_train_2205
[ { "id": "split_0_train_2205_passage", "type": "progene_text", "text": [ "Whereas the WFIKKN gene is expressed primarily in adult pancreas , liver and thymus but not in brain and ovary , significant expression of the WFIKKNRP gene is observed in ovary , testis and brain , but not in liver ." ], "offsets": [ [ 0, 217 ] ] } ]
[ { "id": "split_0_train_3241_entity", "type": "progene_text", "text": [ "WFIKKN" ], "offsets": [ [ 12, 18 ] ], "normalized": [] }, { "id": "split_0_train_3242_entity", "type": "progene_text", "text": [ "WFIKKNRP" ], "offsets": [ [ 143, 151 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2206
split_0_train_2206
[ { "id": "split_0_train_2206_passage", "type": "progene_text", "text": [ "Pronounced differences could also be seen in the case of fetal tissues : expression of the WFIKKN gene was highest in the lung , skeletal muscle and liver , whereas the WFIKKNRP gene was expressed primarily in brain , skeletal muscle , thymus and kidney ." ], "offsets": [ [ 0, 255 ] ] } ]
[ { "id": "split_0_train_3243_entity", "type": "progene_text", "text": [ "WFIKKN" ], "offsets": [ [ 91, 97 ] ], "normalized": [] }, { "id": "split_0_train_3244_entity", "type": "progene_text", "text": [ "WFIKKNRP" ], "offsets": [ [ 169, 177 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2207
split_0_train_2207
[ { "id": "split_0_train_2207_passage", "type": "progene_text", "text": [ "GGA proteins associate with Golgi membranes through interaction between their GGAH domains and ADP-ribosylation factors ." ], "offsets": [ [ 0, 121 ] ] } ]
[ { "id": "split_0_train_3245_entity", "type": "progene_text", "text": [ "GGA" ], "offsets": [ [ 0, 3 ] ], "normalized": [] }, { "id": "split_0_train_3246_entity", "type": "progene_text", "text": [ "ADP-ribosylation factors" ], "offsets": [ [ 95, 119 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2208
split_0_train_2208
[ { "id": "split_0_train_2208_passage", "type": "progene_text", "text": [ "ADP-ribosylation factors ( ARFs ) are a family of small GTPases that are involved in various aspects of membrane trafficking events ." ], "offsets": [ [ 0, 133 ] ] } ]
[ { "id": "split_0_train_3247_entity", "type": "progene_text", "text": [ "ADP-ribosylation factors" ], "offsets": [ [ 0, 24 ] ], "normalized": [] }, { "id": "split_0_train_3248_entity", "type": "progene_text", "text": [ "ARFs" ], "offsets": [ [ 27, 31 ] ], "normalized": [] }, { "id": "split_0_train_3249_entity", "type": "progene_text", "text": [ "small GTPases" ], "offsets": [ [ 50, 63 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2209
split_0_train_2209
[ { "id": "split_0_train_2209_passage", "type": "progene_text", "text": [ "These include ARF1 - ARF6 , which are divided into three classes on the basis of similarity in the primary structure : Class I , ARF1-ARF3 ; Class II , ARF4 and ARF5 ; and Class III , ARF6 ." ], "offsets": [ [ 0, 190 ] ] } ]
[ { "id": "split_0_train_3250_entity", "type": "progene_text", "text": [ "ARF1 - ARF6" ], "offsets": [ [ 14, 25 ] ], "normalized": [] }, { "id": "split_0_train_3251_entity", "type": "progene_text", "text": [ "ARF1-ARF3" ], "offsets": [ [ 129, 138 ] ], "normalized": [] }, { "id": "split_0_train_3252_entity", "type": "progene_text", "text": [ "ARF4" ], "offsets": [ [ 152, 156 ] ], "normalized": [] }, { "id": "split_0_train_3253_entity", "type": "progene_text", "text": [ "ARF5" ], "offsets": [ [ 161, 165 ] ], "normalized": [] }, { "id": "split_0_train_3254_entity", "type": "progene_text", "text": [ "ARF6" ], "offsets": [ [ 184, 188 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2210
split_0_train_2210
[ { "id": "split_0_train_2210_passage", "type": "progene_text", "text": [ "Previous studies identified a novel family of potential ARF effectors , termed GGA1 - GGA3 , which interact specifically with GTP - bound ARF1 and ARF3 and are localized to the trans - Golgi network ( TGN ) or its related compartment (s) ( GGA is an abbreviation for Golgi - localizing , gamma-adaptin ear homology domain , ARF-binding protein ) ." ], "offsets": [ [ 0, 347 ] ] } ]
[ { "id": "split_0_train_3255_entity", "type": "progene_text", "text": [ "ARF" ], "offsets": [ [ 56, 59 ] ], "normalized": [] }, { "id": "split_0_train_3256_entity", "type": "progene_text", "text": [ "GGA1 - GGA3" ], "offsets": [ [ 79, 90 ] ], "normalized": [] }, { "id": "split_0_train_3257_entity", "type": "progene_text", "text": [ "ARF1" ], "offsets": [ [ 138, 142 ] ], "normalized": [] }, { "id": "split_0_train_3258_entity", "type": "progene_text", "text": [ "ARF3" ], "offsets": [ [ 147, 151 ] ], "normalized": [] }, { "id": "split_0_train_3259_entity", "type": "progene_text", "text": [ "GGA" ], "offsets": [ [ 240, 243 ] ], "normalized": [] }, { "id": "split_0_train_3260_entity", "type": "progene_text", "text": [ "Golgi - localizing , gamma-adaptin ear homology domain , ARF-binding protein" ], "offsets": [ [ 267, 343 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2211
split_0_train_2211
[ { "id": "split_0_train_2211_passage", "type": "progene_text", "text": [ "In the present study we have shown that ARF proteins belonging to the three classes , ARF1 , ARF5 and ARF6 , can interact with all GGA proteins in a yeast two - hybrid assay , in vitro and in vivo ." ], "offsets": [ [ 0, 198 ] ] } ]
[ { "id": "split_0_train_3261_entity", "type": "progene_text", "text": [ "ARF" ], "offsets": [ [ 40, 43 ] ], "normalized": [] }, { "id": "split_0_train_3262_entity", "type": "progene_text", "text": [ "ARF1" ], "offsets": [ [ 86, 90 ] ], "normalized": [] }, { "id": "split_0_train_3263_entity", "type": "progene_text", "text": [ "ARF5" ], "offsets": [ [ 93, 97 ] ], "normalized": [] }, { "id": "split_0_train_3264_entity", "type": "progene_text", "text": [ "ARF6" ], "offsets": [ [ 102, 106 ] ], "normalized": [] }, { "id": "split_0_train_3265_entity", "type": "progene_text", "text": [ "GGA" ], "offsets": [ [ 131, 134 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2212
split_0_train_2212
[ { "id": "split_0_train_2212_passage", "type": "progene_text", "text": [ "Segmentation of GGA proteins and isolation of GGA mutants defective in ARF binding have revealed that a limited region within the GGA homology domain , which is conserved in the GGA family , is essential for ARF binding ." ], "offsets": [ [ 0, 221 ] ] } ]
[ { "id": "split_0_train_3266_entity", "type": "progene_text", "text": [ "GGA" ], "offsets": [ [ 16, 19 ] ], "normalized": [] }, { "id": "split_0_train_3267_entity", "type": "progene_text", "text": [ "GGA" ], "offsets": [ [ 46, 49 ] ], "normalized": [] }, { "id": "split_0_train_3268_entity", "type": "progene_text", "text": [ "ARF" ], "offsets": [ [ 71, 74 ] ], "normalized": [] }, { "id": "split_0_train_3269_entity", "type": "progene_text", "text": [ "GGA" ], "offsets": [ [ 130, 133 ] ], "normalized": [] }, { "id": "split_0_train_3270_entity", "type": "progene_text", "text": [ "GGA family" ], "offsets": [ [ 178, 188 ] ], "normalized": [] }, { "id": "split_0_train_3271_entity", "type": "progene_text", "text": [ "ARF" ], "offsets": [ [ 208, 211 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2213
split_0_train_2213
[ { "id": "split_0_train_2213_passage", "type": "progene_text", "text": [ "Expression in cells of GTPase - restricted mutants of ARF1 and ARF5 blocks dissociation of GGA proteins from membranes induced by brefeldin A ." ], "offsets": [ [ 0, 143 ] ] } ]
[ { "id": "split_0_train_3272_entity", "type": "progene_text", "text": [ "GTPase" ], "offsets": [ [ 23, 29 ] ], "normalized": [] }, { "id": "split_0_train_3273_entity", "type": "progene_text", "text": [ "ARF1" ], "offsets": [ [ 54, 58 ] ], "normalized": [] }, { "id": "split_0_train_3274_entity", "type": "progene_text", "text": [ "ARF5" ], "offsets": [ [ 63, 67 ] ], "normalized": [] }, { "id": "split_0_train_3275_entity", "type": "progene_text", "text": [ "GGA" ], "offsets": [ [ 91, 94 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2214
split_0_train_2214
[ { "id": "split_0_train_2214_passage", "type": "progene_text", "text": [ "However , neither of the ARF mutants recruits GGA mutants defective in ARF binding ." ], "offsets": [ [ 0, 84 ] ] } ]
[ { "id": "split_0_train_3276_entity", "type": "progene_text", "text": [ "ARF" ], "offsets": [ [ 25, 28 ] ], "normalized": [] }, { "id": "split_0_train_3277_entity", "type": "progene_text", "text": [ "GGA" ], "offsets": [ [ 46, 49 ] ], "normalized": [] }, { "id": "split_0_train_3278_entity", "type": "progene_text", "text": [ "ARF" ], "offsets": [ [ 71, 74 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2215
split_0_train_2215
[ { "id": "split_0_train_2215_passage", "type": "progene_text", "text": [ "On the basis of these observations , we conclude that at least ARF1 ( Class I ) and ARF5 ( Class II ) in their GTP - bound state cause recruitment of GGA proteins on to TGN membranes ." ], "offsets": [ [ 0, 184 ] ] } ]
[ { "id": "split_0_train_3279_entity", "type": "progene_text", "text": [ "ARF1" ], "offsets": [ [ 63, 67 ] ], "normalized": [] }, { "id": "split_0_train_3280_entity", "type": "progene_text", "text": [ "ARF5" ], "offsets": [ [ 84, 88 ] ], "normalized": [] }, { "id": "split_0_train_3281_entity", "type": "progene_text", "text": [ "GGA" ], "offsets": [ [ 150, 153 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2216
split_0_train_2216
[ { "id": "split_0_train_2216_passage", "type": "progene_text", "text": [ "In contrast , on the basis of similar experiments , ARF6 ( Class III ) may be involved in recruitment of GGA proteins to other compartments , possibly early endosomes ." ], "offsets": [ [ 0, 168 ] ] } ]
[ { "id": "split_0_train_3282_entity", "type": "progene_text", "text": [ "ARF6" ], "offsets": [ [ 52, 56 ] ], "normalized": [] }, { "id": "split_0_train_3283_entity", "type": "progene_text", "text": [ "GGA" ], "offsets": [ [ 105, 108 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2217
split_0_train_2217
[ { "id": "split_0_train_2217_passage", "type": "progene_text", "text": [ "Inhibition of BACE , a promising approach to Alzheimer ' s disease therapy ." ], "offsets": [ [ 0, 76 ] ] } ]
[ { "id": "split_0_train_3284_entity", "type": "progene_text", "text": [ "BACE" ], "offsets": [ [ 14, 18 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2218
split_0_train_2218
[ { "id": "split_0_train_2218_passage", "type": "progene_text", "text": [ "The first proteolytic step in the processing of amyloid precursor protein ( APP ) to amyloid - beta ( Abeta ) in the brain is performed by beta - site APP cleaving enzyme ( BACE1 ) ." ], "offsets": [ [ 0, 182 ] ] } ]
[ { "id": "split_0_train_3285_entity", "type": "progene_text", "text": [ "amyloid precursor protein" ], "offsets": [ [ 48, 73 ] ], "normalized": [] }, { "id": "split_0_train_3286_entity", "type": "progene_text", "text": [ "APP" ], "offsets": [ [ 76, 79 ] ], "normalized": [] }, { "id": "split_0_train_3287_entity", "type": "progene_text", "text": [ "beta - site APP cleaving enzyme" ], "offsets": [ [ 139, 170 ] ], "normalized": [] }, { "id": "split_0_train_3288_entity", "type": "progene_text", "text": [ "BACE1" ], "offsets": [ [ 173, 178 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2219
split_0_train_2219
[ { "id": "split_0_train_2219_passage", "type": "progene_text", "text": [ "This enzyme is a membrane bound aspartic protease with high homology of the catalytic domain to renin and pepsin and of yet unknown physiologic function ." ], "offsets": [ [ 0, 154 ] ] } ]
[ { "id": "split_0_train_3289_entity", "type": "progene_text", "text": [ "aspartic protease" ], "offsets": [ [ 32, 49 ] ], "normalized": [] }, { "id": "split_0_train_3290_entity", "type": "progene_text", "text": [ "renin" ], "offsets": [ [ 96, 101 ] ], "normalized": [] }, { "id": "split_0_train_3291_entity", "type": "progene_text", "text": [ "pepsin" ], "offsets": [ [ 106, 112 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2220
split_0_train_2220
[ { "id": "split_0_train_2220_passage", "type": "progene_text", "text": [ "It is a primary drug discovery target for Alzheimer s disease therapy ." ], "offsets": [ [ 0, 71 ] ] } ]
[]
[]
[]
[]
split_0_train_2221
split_0_train_2221
[ { "id": "split_0_train_2221_passage", "type": "progene_text", "text": [ "The first potent inhibitors are based on the sequence of APP around the beta-secretase cleavage site EVNL / DAEF , with the scissile Leu - Asp amide bond being replaced by a hydroxyethylene transition state analogue isostere ." ], "offsets": [ [ 0, 226 ] ] } ]
[ { "id": "split_0_train_3292_entity", "type": "progene_text", "text": [ "APP" ], "offsets": [ [ 57, 60 ] ], "normalized": [] }, { "id": "split_0_train_3293_entity", "type": "progene_text", "text": [ "beta-secretase" ], "offsets": [ [ 72, 86 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2222
split_0_train_2222
[ { "id": "split_0_train_2222_passage", "type": "progene_text", "text": [ "In addition , lipophilic sidechains have been incorporated and a crystal structure of such an octapeptidic inhibitor bound in the active site is already available ." ], "offsets": [ [ 0, 164 ] ] } ]
[]
[]
[]
[]
split_0_train_2223
split_0_train_2223
[ { "id": "split_0_train_2223_passage", "type": "progene_text", "text": [ "Recent progress in the field of BACE inhibition is reviewed ." ], "offsets": [ [ 0, 61 ] ] } ]
[ { "id": "split_0_train_3294_entity", "type": "progene_text", "text": [ "BACE" ], "offsets": [ [ 32, 36 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2224
split_0_train_2224
[ { "id": "split_0_train_2224_passage", "type": "progene_text", "text": [ "A novel asparaginase - like protein is a sperm autoantigen in rats ." ], "offsets": [ [ 0, 68 ] ] } ]
[ { "id": "split_0_train_3295_entity", "type": "progene_text", "text": [ "asparaginase - like protein" ], "offsets": [ [ 8, 35 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2225
split_0_train_2225
[ { "id": "split_0_train_2225_passage", "type": "progene_text", "text": [ "A novel asparaginase - like protein ( ALP ) of spermatozoa was cloned from rat and human testis cDNA libraries on the basis of reactivity with antibodies produced after vasectomy ." ], "offsets": [ [ 0, 180 ] ] } ]
[ { "id": "split_0_train_3296_entity", "type": "progene_text", "text": [ "asparaginase - like protein" ], "offsets": [ [ 8, 35 ] ], "normalized": [] }, { "id": "split_0_train_3297_entity", "type": "progene_text", "text": [ "ALP" ], "offsets": [ [ 38, 41 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2226
split_0_train_2226
[ { "id": "split_0_train_2226_passage", "type": "progene_text", "text": [ "Although obstruction of the male reproductive tract is known to cause an immunologic response , few of the sperm antigens responsible for the generation of autoantibodies have been characterized ." ], "offsets": [ [ 0, 196 ] ] } ]
[]
[]
[]
[]
split_0_train_2227
split_0_train_2227
[ { "id": "split_0_train_2227_passage", "type": "progene_text", "text": [ "We are identifying proteins of interest by coring autoantigenic protein spots from two - dimensional ( 2-D ) gels of rat sperm extracts and microsequencing them by mass spectrometry ." ], "offsets": [ [ 0, 183 ] ] } ]
[]
[]
[]
[]
split_0_train_2228
split_0_train_2228
[ { "id": "split_0_train_2228_passage", "type": "progene_text", "text": [ "The peptide sequences from ALP , a 28 kDa , pI 5.7 protein , matched to a single partial length rat EST ." ], "offsets": [ [ 0, 105 ] ] } ]
[ { "id": "split_0_train_3298_entity", "type": "progene_text", "text": [ "ALP" ], "offsets": [ [ 27, 30 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2229
split_0_train_2229
[ { "id": "split_0_train_2229_passage", "type": "progene_text", "text": [ "These peptide sequences were used to clone a cDNA encoding a novel 333 amino acid open reading frame ." ], "offsets": [ [ 0, 102 ] ] } ]
[]
[]
[]
[]
split_0_train_2230
split_0_train_2230
[ { "id": "split_0_train_2230_passage", "type": "progene_text", "text": [ "The new protein had a similarity to portions of L-asparaginases of plants ( 43 % ) and to glycosylasparaginases in animal cells ( 32 % ) ." ], "offsets": [ [ 0, 138 ] ] } ]
[ { "id": "split_0_train_3299_entity", "type": "progene_text", "text": [ "L-asparaginases" ], "offsets": [ [ 48, 63 ] ], "normalized": [] }, { "id": "split_0_train_3300_entity", "type": "progene_text", "text": [ "glycosylasparaginases" ], "offsets": [ [ 90, 111 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2231
split_0_train_2231
[ { "id": "split_0_train_2231_passage", "type": "progene_text", "text": [ "Human ALP cDNA was subsequently cloned ." ], "offsets": [ [ 0, 40 ] ] } ]
[ { "id": "split_0_train_3301_entity", "type": "progene_text", "text": [ "ALP" ], "offsets": [ [ 6, 9 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2232
split_0_train_2232
[ { "id": "split_0_train_2232_passage", "type": "progene_text", "text": [ "It showed 77 % identity to the rat ALP sequence and the gene , ASRGL1 ( asparaginase - like 1 ) , mapped to chromosome locus 11q12.3 ." ], "offsets": [ [ 0, 134 ] ] } ]
[ { "id": "split_0_train_3302_entity", "type": "progene_text", "text": [ "ALP" ], "offsets": [ [ 35, 38 ] ], "normalized": [] }, { "id": "split_0_train_3303_entity", "type": "progene_text", "text": [ "ASRGL1" ], "offsets": [ [ 63, 69 ] ], "normalized": [] }, { "id": "split_0_train_3304_entity", "type": "progene_text", "text": [ "asparaginase - like 1" ], "offsets": [ [ 72, 93 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2233
split_0_train_2233
[ { "id": "split_0_train_2233_passage", "type": "progene_text", "text": [ "Purified recombinant rat ALP ( rALP ) , expressed in E. coli , was used to raise polyclonal antiserum in guinea pigs ." ], "offsets": [ [ 0, 118 ] ] } ]
[ { "id": "split_0_train_3305_entity", "type": "progene_text", "text": [ "ALP" ], "offsets": [ [ 25, 28 ] ], "normalized": [] }, { "id": "split_0_train_3306_entity", "type": "progene_text", "text": [ "rALP" ], "offsets": [ [ 31, 35 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2234
split_0_train_2234
[ { "id": "split_0_train_2234_passage", "type": "progene_text", "text": [ "Two observations verified that the correct protein had been cloned : 1 ) the anti - rALP antibody reacted with both rALP and rat sperm ; and 2 ) post - vasectomy sera bound rALP ." ], "offsets": [ [ 0, 179 ] ] } ]
[ { "id": "split_0_train_3307_entity", "type": "progene_text", "text": [ "rALP" ], "offsets": [ [ 84, 88 ] ], "normalized": [] }, { "id": "split_0_train_3308_entity", "type": "progene_text", "text": [ "rALP" ], "offsets": [ [ 116, 120 ] ], "normalized": [] }, { "id": "split_0_train_3309_entity", "type": "progene_text", "text": [ "rALP" ], "offsets": [ [ 173, 177 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2235
split_0_train_2235
[ { "id": "split_0_train_2235_passage", "type": "progene_text", "text": [ "Anti - rALP antibody stained the midpiece of rat and human sperm coincident with staining by MitoTracker Green FM , suggesting that ALP is associated with the mitochondria ." ], "offsets": [ [ 0, 173 ] ] } ]
[ { "id": "split_0_train_3310_entity", "type": "progene_text", "text": [ "rALP" ], "offsets": [ [ 7, 11 ] ], "normalized": [] }, { "id": "split_0_train_3311_entity", "type": "progene_text", "text": [ "ALP" ], "offsets": [ [ 132, 135 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2236
split_0_train_2236
[ { "id": "split_0_train_2236_passage", "type": "progene_text", "text": [ "Northern analysis revealed that rat ALP message was abundantly expressed in the testis but was also present in heart , brain , liver , skeletal muscle , and kidney ." ], "offsets": [ [ 0, 165 ] ] } ]
[ { "id": "split_0_train_3312_entity", "type": "progene_text", "text": [ "ALP" ], "offsets": [ [ 36, 39 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2237
split_0_train_2237
[ { "id": "split_0_train_2237_passage", "type": "progene_text", "text": [ "The XAGE family of cancer / testis - associated genes : alignment and expression profile in normal tissues , melanoma lesions and Ewing 's sarcoma ." ], "offsets": [ [ 0, 148 ] ] } ]
[ { "id": "split_0_train_3313_entity", "type": "progene_text", "text": [ "XAGE family" ], "offsets": [ [ 4, 15 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2238
split_0_train_2238
[ { "id": "split_0_train_2238_passage", "type": "progene_text", "text": [ "The existence of XAGE genes was first reported after database homology searches for PAGE - like sequences identified 3 XAGE EST clusters ." ], "offsets": [ [ 0, 138 ] ] } ]
[ { "id": "split_0_train_3314_entity", "type": "progene_text", "text": [ "XAGE" ], "offsets": [ [ 17, 21 ] ], "normalized": [] }, { "id": "split_0_train_3315_entity", "type": "progene_text", "text": [ "XAGE" ], "offsets": [ [ 119, 123 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2239
split_0_train_2239
[ { "id": "split_0_train_2239_passage", "type": "progene_text", "text": [ "One of these clusters , XAGE-1 , has in later studies been identified as a cancer / testis - associated gene ." ], "offsets": [ [ 0, 110 ] ] } ]
[ { "id": "split_0_train_3316_entity", "type": "progene_text", "text": [ "XAGE-1" ], "offsets": [ [ 24, 30 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2240
split_0_train_2240
[ { "id": "split_0_train_2240_passage", "type": "progene_text", "text": [ "Here , we report the expression profiles of all 3 reported XAGE genes , as well as several splice variants of XAGE-1 , in normal human tissues , Ewing 's sarcoma and melanocytic tumors ." ], "offsets": [ [ 0, 186 ] ] } ]
[ { "id": "split_0_train_3317_entity", "type": "progene_text", "text": [ "XAGE" ], "offsets": [ [ 59, 63 ] ], "normalized": [] }, { "id": "split_0_train_3318_entity", "type": "progene_text", "text": [ "XAGE-1" ], "offsets": [ [ 110, 116 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2241
split_0_train_2241
[ { "id": "split_0_train_2241_passage", "type": "progene_text", "text": [ "We also provide the genetic structure of the corresponding genes ." ], "offsets": [ [ 0, 66 ] ] } ]
[]
[]
[]
[]
split_0_train_2242
split_0_train_2242
[ { "id": "split_0_train_2242_passage", "type": "progene_text", "text": [ "Moreover , by searching the databases for XAGE homologues , we identified 3 additional GAGE - like genes ." ], "offsets": [ [ 0, 106 ] ] } ]
[ { "id": "split_0_train_3319_entity", "type": "progene_text", "text": [ "XAGE" ], "offsets": [ [ 42, 46 ] ], "normalized": [] }, { "id": "split_0_train_3320_entity", "type": "progene_text", "text": [ "GAGE" ], "offsets": [ [ 87, 91 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2243
split_0_train_2243
[ { "id": "split_0_train_2243_passage", "type": "progene_text", "text": [ "RT - PCR studies showed frequent expression in melanoma metastases and Ewing 's sarcoma for 2 XAGE-1 - derived transcripts ." ], "offsets": [ [ 0, 124 ] ] } ]
[ { "id": "split_0_train_3321_entity", "type": "progene_text", "text": [ "XAGE-1" ], "offsets": [ [ 94, 100 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2244
split_0_train_2244
[ { "id": "split_0_train_2244_passage", "type": "progene_text", "text": [ "XAGE-2 was expressed at lower frequency in these tissues , while XAGE-3 was seen only in normal placenta ." ], "offsets": [ [ 0, 106 ] ] } ]
[ { "id": "split_0_train_3322_entity", "type": "progene_text", "text": [ "XAGE-2" ], "offsets": [ [ 0, 6 ] ], "normalized": [] }, { "id": "split_0_train_3323_entity", "type": "progene_text", "text": [ "XAGE-3" ], "offsets": [ [ 65, 71 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2245
split_0_train_2245
[ { "id": "split_0_train_2245_passage", "type": "progene_text", "text": [ "Due to a frameshift , the largest XAGE-1 putative protein is far less homologous to GAGE - like proteins than the other XAGEs ." ], "offsets": [ [ 0, 127 ] ] } ]
[ { "id": "split_0_train_3324_entity", "type": "progene_text", "text": [ "XAGE-1" ], "offsets": [ [ 34, 40 ] ], "normalized": [] }, { "id": "split_0_train_3325_entity", "type": "progene_text", "text": [ "GAGE" ], "offsets": [ [ 84, 88 ] ], "normalized": [] }, { "id": "split_0_train_3326_entity", "type": "progene_text", "text": [ "XAGEs" ], "offsets": [ [ 120, 125 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2246
split_0_train_2246
[ { "id": "split_0_train_2246_passage", "type": "progene_text", "text": [ "Interestingly , all GAGE - like genes contain a large secondary open reading frame , coding for putative proteins homologues to the XAGE-1 primary protein ." ], "offsets": [ [ 0, 156 ] ] } ]
[ { "id": "split_0_train_3327_entity", "type": "progene_text", "text": [ "GAGE" ], "offsets": [ [ 20, 24 ] ], "normalized": [] }, { "id": "split_0_train_3328_entity", "type": "progene_text", "text": [ "XAGE-1" ], "offsets": [ [ 132, 138 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2247
split_0_train_2247
[ { "id": "split_0_train_2247_passage", "type": "progene_text", "text": [ "The XAGE family of cancer / testis - associated genes is located on chromosome Xp11.21 - Xp11.22 ." ], "offsets": [ [ 0, 98 ] ] } ]
[ { "id": "split_0_train_3329_entity", "type": "progene_text", "text": [ "XAGE family" ], "offsets": [ [ 4, 15 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2248
split_0_train_2248
[ { "id": "split_0_train_2248_passage", "type": "progene_text", "text": [ "The data outline a superfamily of GAGE - like cancer / testis antigens , consisting of at least 19 genes ." ], "offsets": [ [ 0, 106 ] ] } ]
[ { "id": "split_0_train_3330_entity", "type": "progene_text", "text": [ "superfamily of GAGE - like cancer / testis antigens" ], "offsets": [ [ 19, 70 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2249
split_0_train_2249
[ { "id": "split_0_train_2249_passage", "type": "progene_text", "text": [ "Novel intercellular communication system in Escherichia coli that confers antibiotic resistance between physically separated populations ." ], "offsets": [ [ 0, 138 ] ] } ]
[]
[]
[]
[]
split_0_train_2250
split_0_train_2250
[ { "id": "split_0_train_2250_passage", "type": "progene_text", "text": [ "AIMS :" ], "offsets": [ [ 0, 6 ] ] } ]
[]
[]
[]
[]
split_0_train_2251
split_0_train_2251
[ { "id": "split_0_train_2251_passage", "type": "progene_text", "text": [ "To determine whether intercellular signalling can occur between physically separated populations of Escherichia coli ." ], "offsets": [ [ 0, 118 ] ] } ]
[]
[]
[]
[]
split_0_train_2252
split_0_train_2252
[ { "id": "split_0_train_2252_passage", "type": "progene_text", "text": [ "METHODS AND RESULTS :" ], "offsets": [ [ 0, 21 ] ] } ]
[]
[]
[]
[]
split_0_train_2253
split_0_train_2253
[ { "id": "split_0_train_2253_passage", "type": "progene_text", "text": [ "Intercellular signalling between physically discrete populations of E. coli BL21 was analysed in bi - partite Petri dishes ." ], "offsets": [ [ 0, 124 ] ] } ]
[]
[]
[]
[]
split_0_train_2254
split_0_train_2254
[ { "id": "split_0_train_2254_passage", "type": "progene_text", "text": [ "Transfer of a growth - promoting signal resulted in induction of resistance to the antibiotic ampicillin ." ], "offsets": [ [ 0, 106 ] ] } ]
[]
[]
[]
[]
split_0_train_2255
split_0_train_2255
[ { "id": "split_0_train_2255_passage", "type": "progene_text", "text": [ "Optimal expression of the signal occurred when the signalling population was established as a bacterial lawn for 24 h ." ], "offsets": [ [ 0, 119 ] ] } ]
[]
[]
[]
[]
split_0_train_2256
split_0_train_2256
[ { "id": "split_0_train_2256_passage", "type": "progene_text", "text": [ "This represented an entry into the stationary phase of growth , as indicated by the expression profile of the RNA polymerase subunit sigma38 ( sigmaS ; sigma S ) ." ], "offsets": [ [ 0, 163 ] ] } ]
[ { "id": "split_0_train_3331_entity", "type": "progene_text", "text": [ "RNA polymerase subunit sigma38" ], "offsets": [ [ 110, 140 ] ], "normalized": [] }, { "id": "split_0_train_3332_entity", "type": "progene_text", "text": [ "sigmaS" ], "offsets": [ [ 143, 149 ] ], "normalized": [] }, { "id": "split_0_train_3333_entity", "type": "progene_text", "text": [ "sigma S" ], "offsets": [ [ 152, 159 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2257
split_0_train_2257
[ { "id": "split_0_train_2257_passage", "type": "progene_text", "text": [ "The growth - promoting effect was also observed when E. coli DH5alpha ( luxS - ) was used as the signalling population ." ], "offsets": [ [ 0, 120 ] ] } ]
[ { "id": "split_0_train_3334_entity", "type": "progene_text", "text": [ "luxS" ], "offsets": [ [ 72, 76 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2258
split_0_train_2258
[ { "id": "split_0_train_2258_passage", "type": "progene_text", "text": [ "Preventing passage of air between the two populations resulted in a complete cessation of the growth - promoting effect ." ], "offsets": [ [ 0, 121 ] ] } ]
[]
[]
[]
[]
split_0_train_2259
split_0_train_2259
[ { "id": "split_0_train_2259_passage", "type": "progene_text", "text": [ "CONCLUSIONS :" ], "offsets": [ [ 0, 13 ] ] } ]
[]
[]
[]
[]
split_0_train_2260
split_0_train_2260
[ { "id": "split_0_train_2260_passage", "type": "progene_text", "text": [ "A growth - promoting signal occurs between physically separated cultures of E. coli ." ], "offsets": [ [ 0, 85 ] ] } ]
[]
[]
[]
[]
split_0_train_2261
split_0_train_2261
[ { "id": "split_0_train_2261_passage", "type": "progene_text", "text": [ "The exact nature of the signal remains to be determined but does not involve the production of autoinducer-2 from the luxS gene ." ], "offsets": [ [ 0, 129 ] ] } ]
[ { "id": "split_0_train_3335_entity", "type": "progene_text", "text": [ "luxS" ], "offsets": [ [ 118, 122 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2262
split_0_train_2262
[ { "id": "split_0_train_2262_passage", "type": "progene_text", "text": [ "Signal transmission is likely to involve airborne transfer of a signal species ." ], "offsets": [ [ 0, 80 ] ] } ]
[]
[]
[]
[]
split_0_train_2263
split_0_train_2263
[ { "id": "split_0_train_2263_passage", "type": "progene_text", "text": [ "SIGNIFICANCE AND IMPACT OF THE STUDY :" ], "offsets": [ [ 0, 38 ] ] } ]
[]
[]
[]
[]
split_0_train_2264
split_0_train_2264
[ { "id": "split_0_train_2264_passage", "type": "progene_text", "text": [ "Intercellular signalling systems exist in bacteria that enable antibiotic resistance to be conferred between physically separated populations ." ], "offsets": [ [ 0, 143 ] ] } ]
[]
[]
[]
[]
split_0_train_2265
split_0_train_2265
[ { "id": "split_0_train_2265_passage", "type": "progene_text", "text": [ "PYPAF7 , a novel PYRIN - containing Apaf1 - like protein that regulates activation of NF-kappa B and caspase-1 - dependent cytokine processing ." ], "offsets": [ [ 0, 144 ] ] } ]
[ { "id": "split_0_train_3336_entity", "type": "progene_text", "text": [ "PYPAF7" ], "offsets": [ [ 0, 6 ] ], "normalized": [] }, { "id": "split_0_train_3337_entity", "type": "progene_text", "text": [ "PYRIN - containing Apaf1 - like protein" ], "offsets": [ [ 17, 56 ] ], "normalized": [] }, { "id": "split_0_train_3338_entity", "type": "progene_text", "text": [ "NF-kappa B" ], "offsets": [ [ 86, 96 ] ], "normalized": [] }, { "id": "split_0_train_3339_entity", "type": "progene_text", "text": [ "caspase-1" ], "offsets": [ [ 101, 110 ] ], "normalized": [] }, { "id": "split_0_train_3340_entity", "type": "progene_text", "text": [ "cytokine" ], "offsets": [ [ 123, 131 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2266
split_0_train_2266
[ { "id": "split_0_train_2266_passage", "type": "progene_text", "text": [ "PYRIN - containing Apaf1 - like proteins ( PYPAFs ) are members of the nucleotide - binding site / leucine - rich repeat ( NBS / LRR ) family of signal transduction proteins ." ], "offsets": [ [ 0, 175 ] ] } ]
[ { "id": "split_0_train_3341_entity", "type": "progene_text", "text": [ "PYRIN - containing Apaf1 - like proteins" ], "offsets": [ [ 0, 40 ] ], "normalized": [] }, { "id": "split_0_train_3342_entity", "type": "progene_text", "text": [ "PYPAFs" ], "offsets": [ [ 43, 49 ] ], "normalized": [] }, { "id": "split_0_train_3343_entity", "type": "progene_text", "text": [ "nucleotide - binding site / leucine - rich repeat ( NBS / LRR ) family" ], "offsets": [ [ 71, 141 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2267
split_0_train_2267
[ { "id": "split_0_train_2267_passage", "type": "progene_text", "text": [ "We report here that PYPAF7 is a novel PYPAF protein that activates inflammatory signaling pathways ." ], "offsets": [ [ 0, 100 ] ] } ]
[ { "id": "split_0_train_3344_entity", "type": "progene_text", "text": [ "PYPAF7" ], "offsets": [ [ 20, 26 ] ], "normalized": [] }, { "id": "split_0_train_3345_entity", "type": "progene_text", "text": [ "PYPAF" ], "offsets": [ [ 38, 43 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2268
split_0_train_2268
[ { "id": "split_0_train_2268_passage", "type": "progene_text", "text": [ "The expression of PYPAF7 is highly restricted to immune cells , and its gene maps to chromosome 19q13.4 , a locus that contains a cluster of genes encoding numerous PYPAF family members ." ], "offsets": [ [ 0, 187 ] ] } ]
[ { "id": "split_0_train_3346_entity", "type": "progene_text", "text": [ "PYPAF7" ], "offsets": [ [ 18, 24 ] ], "normalized": [] }, { "id": "split_0_train_3347_entity", "type": "progene_text", "text": [ "PYPAF family" ], "offsets": [ [ 165, 177 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2269
split_0_train_2269
[ { "id": "split_0_train_2269_passage", "type": "progene_text", "text": [ "Co - expression of PYPAF7 with ASC results in the recruitment of PYPAF7 to distinct cytoplasmic loci and a potent synergistic activation of NF-kappa B ." ], "offsets": [ [ 0, 152 ] ] } ]
[ { "id": "split_0_train_3348_entity", "type": "progene_text", "text": [ "PYPAF7" ], "offsets": [ [ 19, 25 ] ], "normalized": [] }, { "id": "split_0_train_3349_entity", "type": "progene_text", "text": [ "ASC" ], "offsets": [ [ 31, 34 ] ], "normalized": [] }, { "id": "split_0_train_3350_entity", "type": "progene_text", "text": [ "PYPAF7" ], "offsets": [ [ 65, 71 ] ], "normalized": [] }, { "id": "split_0_train_3351_entity", "type": "progene_text", "text": [ "NF-kappa B" ], "offsets": [ [ 140, 150 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2270
split_0_train_2270
[ { "id": "split_0_train_2270_passage", "type": "progene_text", "text": [ "To identify other proteins involved in PYPAF7 and ASC signaling pathways , we performed a mammalian two - hybrid screen and identified pro - caspase-1 as a binding partner of ASC ." ], "offsets": [ [ 0, 180 ] ] } ]
[ { "id": "split_0_train_3352_entity", "type": "progene_text", "text": [ "PYPAF7" ], "offsets": [ [ 39, 45 ] ], "normalized": [] }, { "id": "split_0_train_3353_entity", "type": "progene_text", "text": [ "ASC" ], "offsets": [ [ 50, 53 ] ], "normalized": [] }, { "id": "split_0_train_3354_entity", "type": "progene_text", "text": [ "caspase-1" ], "offsets": [ [ 141, 150 ] ], "normalized": [] }, { "id": "split_0_train_3355_entity", "type": "progene_text", "text": [ "ASC" ], "offsets": [ [ 175, 178 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2271
split_0_train_2271
[ { "id": "split_0_train_2271_passage", "type": "progene_text", "text": [ "Co - expression of PYPAF7 and ASC results in the synergistic activation of caspase-1 and a corresponding increase in secretion of interleukin-1 beta ." ], "offsets": [ [ 0, 150 ] ] } ]
[ { "id": "split_0_train_3356_entity", "type": "progene_text", "text": [ "PYPAF7" ], "offsets": [ [ 19, 25 ] ], "normalized": [] }, { "id": "split_0_train_3357_entity", "type": "progene_text", "text": [ "ASC" ], "offsets": [ [ 30, 33 ] ], "normalized": [] }, { "id": "split_0_train_3358_entity", "type": "progene_text", "text": [ "caspase-1" ], "offsets": [ [ 75, 84 ] ], "normalized": [] }, { "id": "split_0_train_3359_entity", "type": "progene_text", "text": [ "interleukin-1 beta" ], "offsets": [ [ 130, 148 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2272
split_0_train_2272
[ { "id": "split_0_train_2272_passage", "type": "progene_text", "text": [ "In addition , PYPAF1 induces caspase-1 - dependent cytokine processing when co - expressed with ASC ." ], "offsets": [ [ 0, 101 ] ] } ]
[ { "id": "split_0_train_3360_entity", "type": "progene_text", "text": [ "PYPAF1" ], "offsets": [ [ 14, 20 ] ], "normalized": [] }, { "id": "split_0_train_3361_entity", "type": "progene_text", "text": [ "caspase-1" ], "offsets": [ [ 29, 38 ] ], "normalized": [] }, { "id": "split_0_train_3362_entity", "type": "progene_text", "text": [ "cytokine" ], "offsets": [ [ 51, 59 ] ], "normalized": [] }, { "id": "split_0_train_3363_entity", "type": "progene_text", "text": [ "ASC" ], "offsets": [ [ 96, 99 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2273
split_0_train_2273
[ { "id": "split_0_train_2273_passage", "type": "progene_text", "text": [ "These findings indicate that PYPAF family members participate in inflammatory signaling by regulating the activation of NF-kappa B and cytokine processing ." ], "offsets": [ [ 0, 156 ] ] } ]
[ { "id": "split_0_train_3364_entity", "type": "progene_text", "text": [ "PYPAF family" ], "offsets": [ [ 29, 41 ] ], "normalized": [] }, { "id": "split_0_train_3365_entity", "type": "progene_text", "text": [ "NF-kappa B" ], "offsets": [ [ 120, 130 ] ], "normalized": [] }, { "id": "split_0_train_3366_entity", "type": "progene_text", "text": [ "cytokine" ], "offsets": [ [ 135, 143 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2274
split_0_train_2274
[ { "id": "split_0_train_2274_passage", "type": "progene_text", "text": [ "Metallochaperone Atox1 transfers copper to the NH2 - terminal domain of the Wilson 's disease protein and regulates its catalytic activity ." ], "offsets": [ [ 0, 140 ] ] } ]
[ { "id": "split_0_train_3367_entity", "type": "progene_text", "text": [ "Metallochaperone" ], "offsets": [ [ 0, 16 ] ], "normalized": [] }, { "id": "split_0_train_3368_entity", "type": "progene_text", "text": [ "Atox1" ], "offsets": [ [ 17, 22 ] ], "normalized": [] }, { "id": "split_0_train_3369_entity", "type": "progene_text", "text": [ "Wilson 's disease protein" ], "offsets": [ [ 76, 101 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2275
split_0_train_2275
[ { "id": "split_0_train_2275_passage", "type": "progene_text", "text": [ "Copper is essential for the growth and development of mammalian cells ." ], "offsets": [ [ 0, 71 ] ] } ]
[]
[]
[]
[]
split_0_train_2276
split_0_train_2276
[ { "id": "split_0_train_2276_passage", "type": "progene_text", "text": [ "The key role in the intracellular distribution of copper belongs to the recently discovered family of metallochaperones and to copper - transporting P - type ATPases ." ], "offsets": [ [ 0, 167 ] ] } ]
[ { "id": "split_0_train_3370_entity", "type": "progene_text", "text": [ "metallochaperones" ], "offsets": [ [ 102, 119 ] ], "normalized": [] }, { "id": "split_0_train_3371_entity", "type": "progene_text", "text": [ "copper - transporting P - type ATPases" ], "offsets": [ [ 127, 165 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2277
split_0_train_2277
[ { "id": "split_0_train_2277_passage", "type": "progene_text", "text": [ "The mutations in the ATPase ATP7B , the Wilson 's disease protein ( WNDP ) , lead to intracellular accumulation of copper and severe hepatic and neurological abnormalities ." ], "offsets": [ [ 0, 173 ] ] } ]
[ { "id": "split_0_train_3372_entity", "type": "progene_text", "text": [ "ATPase" ], "offsets": [ [ 21, 27 ] ], "normalized": [] }, { "id": "split_0_train_3373_entity", "type": "progene_text", "text": [ "ATP7B" ], "offsets": [ [ 28, 33 ] ], "normalized": [] }, { "id": "split_0_train_3374_entity", "type": "progene_text", "text": [ "Wilson 's disease protein" ], "offsets": [ [ 40, 65 ] ], "normalized": [] }, { "id": "split_0_train_3375_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 68, 72 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2278
split_0_train_2278
[ { "id": "split_0_train_2278_passage", "type": "progene_text", "text": [ "Several of these mutations were shown to disrupt the protein - protein interactions between WNDP and the metallochaperone Atox1 , suggesting that these interactions are important for normal copper homeostasis ." ], "offsets": [ [ 0, 210 ] ] } ]
[ { "id": "split_0_train_3376_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 92, 96 ] ], "normalized": [] }, { "id": "split_0_train_3377_entity", "type": "progene_text", "text": [ "metallochaperone" ], "offsets": [ [ 105, 121 ] ], "normalized": [] }, { "id": "split_0_train_3378_entity", "type": "progene_text", "text": [ "Atox1" ], "offsets": [ [ 122, 127 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2279
split_0_train_2279
[ { "id": "split_0_train_2279_passage", "type": "progene_text", "text": [ "To understand the functional consequences of the Atox1 - WNDP interaction at the molecular level , we produced recombinant Atox1 and characterized its effects on WNDP ." ], "offsets": [ [ 0, 168 ] ] } ]
[ { "id": "split_0_train_3379_entity", "type": "progene_text", "text": [ "Atox1" ], "offsets": [ [ 49, 54 ] ], "normalized": [] }, { "id": "split_0_train_3380_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 57, 61 ] ], "normalized": [] }, { "id": "split_0_train_3381_entity", "type": "progene_text", "text": [ "Atox1" ], "offsets": [ [ 123, 128 ] ], "normalized": [] }, { "id": "split_0_train_3382_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 162, 166 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2280
split_0_train_2280
[ { "id": "split_0_train_2280_passage", "type": "progene_text", "text": [ "We demonstrate that Atox1 transfers copper to the purified amino - terminal domain of WNDP ( N - WNDP ) in a dose - dependent and saturable manner ." ], "offsets": [ [ 0, 148 ] ] } ]
[ { "id": "split_0_train_3383_entity", "type": "progene_text", "text": [ "Atox1" ], "offsets": [ [ 20, 25 ] ], "normalized": [] }, { "id": "split_0_train_3384_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 86, 90 ] ], "normalized": [] }, { "id": "split_0_train_3385_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 97, 101 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2281
split_0_train_2281
[ { "id": "split_0_train_2281_passage", "type": "progene_text", "text": [ "A maximum of six copper atoms can be transferred to N - WNDP by the chaperone ." ], "offsets": [ [ 0, 79 ] ] } ]
[ { "id": "split_0_train_3386_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 56, 60 ] ], "normalized": [] }, { "id": "split_0_train_3387_entity", "type": "progene_text", "text": [ "chaperone" ], "offsets": [ [ 68, 77 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2282
split_0_train_2282
[ { "id": "split_0_train_2282_passage", "type": "progene_text", "text": [ "Furthermore , the incubation of copper Atox1 with the full - length WNDP leads to the stimulation of the WNDP catalytic activity , providing strong evidence for the direct effect of Atox1 on the function of this transporter ." ], "offsets": [ [ 0, 225 ] ] } ]
[ { "id": "split_0_train_3388_entity", "type": "progene_text", "text": [ "Atox1" ], "offsets": [ [ 39, 44 ] ], "normalized": [] }, { "id": "split_0_train_3389_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 68, 72 ] ], "normalized": [] }, { "id": "split_0_train_3390_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 105, 109 ] ], "normalized": [] }, { "id": "split_0_train_3391_entity", "type": "progene_text", "text": [ "Atox1" ], "offsets": [ [ 182, 187 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2283
split_0_train_2283
[ { "id": "split_0_train_2283_passage", "type": "progene_text", "text": [ "Our data also suggest that Atox1 can regulate the copper occupancy of WNDP ." ], "offsets": [ [ 0, 76 ] ] } ]
[ { "id": "split_0_train_3392_entity", "type": "progene_text", "text": [ "Atox1" ], "offsets": [ [ 27, 32 ] ], "normalized": [] }, { "id": "split_0_train_3393_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 70, 74 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2284
split_0_train_2284
[ { "id": "split_0_train_2284_passage", "type": "progene_text", "text": [ "The incubation with apo - Atox1 results in the removal of copper from the metalated N - WNDP and apparent down - regulation of WNDP activity ." ], "offsets": [ [ 0, 142 ] ] } ]
[ { "id": "split_0_train_3394_entity", "type": "progene_text", "text": [ "Atox1" ], "offsets": [ [ 26, 31 ] ], "normalized": [] }, { "id": "split_0_train_3395_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 88, 92 ] ], "normalized": [] }, { "id": "split_0_train_3396_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 127, 131 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2285
split_0_train_2285
[ { "id": "split_0_train_2285_passage", "type": "progene_text", "text": [ "Interestingly , at least one copper atom remains tightly bound to N - WNDP even in the presence of excess apo - Atox1 ." ], "offsets": [ [ 0, 119 ] ] } ]
[ { "id": "split_0_train_3397_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 70, 74 ] ], "normalized": [] }, { "id": "split_0_train_3398_entity", "type": "progene_text", "text": [ "Atox1" ], "offsets": [ [ 112, 117 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2286
split_0_train_2286
[ { "id": "split_0_train_2286_passage", "type": "progene_text", "text": [ "We suggest that this incomplete reversibility reflects the functional non - equivalency of the metal - binding sites in WNDP and speculate about the intracellular consequences of the reversible Atox1 - mediated copper transfer ." ], "offsets": [ [ 0, 228 ] ] } ]
[ { "id": "split_0_train_3399_entity", "type": "progene_text", "text": [ "WNDP" ], "offsets": [ [ 120, 124 ] ], "normalized": [] }, { "id": "split_0_train_3400_entity", "type": "progene_text", "text": [ "Atox1" ], "offsets": [ [ 194, 199 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2287
split_0_train_2287
[ { "id": "split_0_train_2287_passage", "type": "progene_text", "text": [ "Significance of the parkin gene and protein in understanding Parkinson 's disease ." ], "offsets": [ [ 0, 83 ] ] } ]
[ { "id": "split_0_train_3401_entity", "type": "progene_text", "text": [ "parkin" ], "offsets": [ [ 20, 26 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2288
split_0_train_2288
[ { "id": "split_0_train_2288_passage", "type": "progene_text", "text": [ "Mutations in the parkin gene cause autosomal recessive inherited juvenile parkinsonism ( ARJP ) and account for the majority of cases of inherited Parkinson 's disease ( PD ) of young onset ( < 45 years of age ) ." ], "offsets": [ [ 0, 213 ] ] } ]
[ { "id": "split_0_train_3402_entity", "type": "progene_text", "text": [ "parkin" ], "offsets": [ [ 17, 23 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2289
split_0_train_2289
[ { "id": "split_0_train_2289_passage", "type": "progene_text", "text": [ "Patients with parkin mutations commonly have atypical clinical features such as dystonia at onset , hyper - reflexia , diurnal fluctuations , and sleep benefit ; however , parkin mutation patients with both typical PD symptoms and older age of onset have been identified ." ], "offsets": [ [ 0, 272 ] ] } ]
[ { "id": "split_0_train_3403_entity", "type": "progene_text", "text": [ "parkin" ], "offsets": [ [ 14, 20 ] ], "normalized": [] }, { "id": "split_0_train_3404_entity", "type": "progene_text", "text": [ "parkin" ], "offsets": [ [ 172, 178 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2290
split_0_train_2290
[ { "id": "split_0_train_2290_passage", "type": "progene_text", "text": [ "Parkin is a ubiquitin protein ligase ( E3 ) , a component in the pathway that attaches ubiquitin to specific proteins , designating them for degradation by the proteasome ." ], "offsets": [ [ 0, 172 ] ] } ]
[ { "id": "split_0_train_3405_entity", "type": "progene_text", "text": [ "Parkin" ], "offsets": [ [ 0, 6 ] ], "normalized": [] }, { "id": "split_0_train_3406_entity", "type": "progene_text", "text": [ "ubiquitin protein ligase ( E3 )" ], "offsets": [ [ 12, 43 ] ], "normalized": [] }, { "id": "split_0_train_3407_entity", "type": "progene_text", "text": [ "ubiquitin" ], "offsets": [ [ 87, 96 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2291
split_0_train_2291
[ { "id": "split_0_train_2291_passage", "type": "progene_text", "text": [ "Several substrates for parkin have been identified ( CDCrel-1 , o - glycosylated alpha-synuclein , parkin associated endothelin - like cell receptor , and synphilin ) ." ], "offsets": [ [ 0, 168 ] ] } ]
[ { "id": "split_0_train_3408_entity", "type": "progene_text", "text": [ "parkin" ], "offsets": [ [ 23, 29 ] ], "normalized": [] }, { "id": "split_0_train_3409_entity", "type": "progene_text", "text": [ "CDCrel-1" ], "offsets": [ [ 53, 61 ] ], "normalized": [] }, { "id": "split_0_train_3410_entity", "type": "progene_text", "text": [ "alpha-synuclein" ], "offsets": [ [ 81, 96 ] ], "normalized": [] }, { "id": "split_0_train_3411_entity", "type": "progene_text", "text": [ "parkin associated endothelin - like cell receptor" ], "offsets": [ [ 99, 148 ] ], "normalized": [] }, { "id": "split_0_train_3412_entity", "type": "progene_text", "text": [ "synphilin" ], "offsets": [ [ 155, 164 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2292
split_0_train_2292
[ { "id": "split_0_train_2292_passage", "type": "progene_text", "text": [ "The role of these substrates in the pathogenesis of ARJP is under active study ." ], "offsets": [ [ 0, 80 ] ] } ]
[]
[]
[]
[]
split_0_train_2293
split_0_train_2293
[ { "id": "split_0_train_2293_passage", "type": "progene_text", "text": [ "Most patients with parkin mutations lack Lewy bodies , suggesting that functional parkin is involved in the formation of these highly ubiquitinated inclusions ." ], "offsets": [ [ 0, 160 ] ] } ]
[ { "id": "split_0_train_3413_entity", "type": "progene_text", "text": [ "parkin" ], "offsets": [ [ 19, 25 ] ], "normalized": [] }, { "id": "split_0_train_3414_entity", "type": "progene_text", "text": [ "parkin" ], "offsets": [ [ 82, 88 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2294
split_0_train_2294
[ { "id": "split_0_train_2294_passage", "type": "progene_text", "text": [ "Furthermore , the recognition that parkin mutations can lead to a disorder clinically similar to sporadic PD , but presumably lacking Lewy bodies , calls into question the necessity of Lewy bodies for the diagnosis of PD and nigral cell death ." ], "offsets": [ [ 0, 244 ] ] } ]
[ { "id": "split_0_train_3415_entity", "type": "progene_text", "text": [ "parkin" ], "offsets": [ [ 35, 41 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2295
split_0_train_2295
[ { "id": "split_0_train_2295_passage", "type": "progene_text", "text": [ "Studies of parkin are increasing the focus on the role of the ubiquitin - proteasome system in the pathogenesis of both familial and sporadic PD ." ], "offsets": [ [ 0, 146 ] ] } ]
[ { "id": "split_0_train_3416_entity", "type": "progene_text", "text": [ "parkin" ], "offsets": [ [ 11, 17 ] ], "normalized": [] }, { "id": "split_0_train_3417_entity", "type": "progene_text", "text": [ "ubiquitin" ], "offsets": [ [ 62, 71 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2296
split_0_train_2296
[ { "id": "split_0_train_2296_passage", "type": "progene_text", "text": [ "Phospholipase C-beta 2 interacts with mitogen - activated protein kinase kinase 3 ." ], "offsets": [ [ 0, 83 ] ] } ]
[ { "id": "split_0_train_3418_entity", "type": "progene_text", "text": [ "Phospholipase C-beta 2" ], "offsets": [ [ 0, 22 ] ], "normalized": [] }, { "id": "split_0_train_3419_entity", "type": "progene_text", "text": [ "mitogen - activated protein kinase kinase 3" ], "offsets": [ [ 38, 81 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2297
split_0_train_2297
[ { "id": "split_0_train_2297_passage", "type": "progene_text", "text": [ "Phospholipase C ( PLC ) - beta enzymes ( isoenzymes beta 1-beta 4 ) are activated by G protein subunits , leading to the generation of intracellular messengers which mobilize calcium and activate protein kinase C ." ], "offsets": [ [ 0, 214 ] ] } ]
[ { "id": "split_0_train_3420_entity", "type": "progene_text", "text": [ "Phospholipase C ( PLC ) - beta" ], "offsets": [ [ 0, 30 ] ], "normalized": [] }, { "id": "split_0_train_3421_entity", "type": "progene_text", "text": [ "G protein" ], "offsets": [ [ 85, 94 ] ], "normalized": [] }, { "id": "split_0_train_3422_entity", "type": "progene_text", "text": [ "protein kinase C" ], "offsets": [ [ 196, 212 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2298
split_0_train_2298
[ { "id": "split_0_train_2298_passage", "type": "progene_text", "text": [ "It has recently been recognized that these enzymes interact with and are regulated by proteins other than G proteins ." ], "offsets": [ [ 0, 118 ] ] } ]
[ { "id": "split_0_train_3423_entity", "type": "progene_text", "text": [ "G proteins" ], "offsets": [ [ 106, 116 ] ], "normalized": [] } ]
[]
[]
[]
split_0_train_2299
split_0_train_2299
[ { "id": "split_0_train_2299_passage", "type": "progene_text", "text": [ "Using the yeast two - hybrid technique to screen a leukocyte library we identified mitogen - activated protein kinase kinase 3 ( MKK3 ) as a partner of PLC-beta 2 ." ], "offsets": [ [ 0, 164 ] ] } ]
[ { "id": "split_0_train_3424_entity", "type": "progene_text", "text": [ "mitogen - activated protein kinase kinase 3" ], "offsets": [ [ 83, 126 ] ], "normalized": [] }, { "id": "split_0_train_3425_entity", "type": "progene_text", "text": [ "MKK3" ], "offsets": [ [ 129, 133 ] ], "normalized": [] }, { "id": "split_0_train_3426_entity", "type": "progene_text", "text": [ "PLC-beta 2" ], "offsets": [ [ 152, 162 ] ], "normalized": [] } ]
[]
[]
[]