> top > docs > PubMed:8636252 > annotations

PubMed:8636252 JSONTXT

Annnotations TAB JSON ListView MergeView

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease:D000326 denotes X-linked adrenoleukodystrophy
T2 64-81 SpecificDisease:D000224 denotes Addison's disease
T3 112-141 SpecificDisease:D000326 denotes X-Linked adrenoleukodystrophy
T4 143-146 SpecificDisease:D000326 denotes ALD
T5 153-168 DiseaseClass:D030342 denotes genetic disease
T6 185-228 DiseaseClass:D020279 denotes demyelination of the central nervous system
T7 230-251 DiseaseClass:D000309 denotes adrenal insufficiency
T8 328-331 SpecificDisease:D000326 denotes ALD
T9 474-477 SpecificDisease:D000326 denotes ALD
T10 544-565 SpecificDisease:D000326 denotes Adrenomyeloneuropathy
T11 567-570 SpecificDisease:D000326 denotes AMN
T12 642-663 DiseaseClass:D000309 denotes Adrenal insufficiency
T13 665-682 SpecificDisease:D000224 denotes Addison's disease
T14 714-717 SpecificDisease:D000326 denotes AMN
T15 721-733 SpecificDisease:D000326 denotes cerebral ALD
T16 781-784 SpecificDisease:D000326 denotes ALD
T17 818-821 SpecificDisease:D000326 denotes ALD
T18 840-857 SpecificDisease:D000224 denotes Addison's disease
T19 1080-1108 DiseaseClass:D000224 denotes adrenocortical insufficiency
T20 1369-1381 SpecificDisease:D000326 denotes cerebral ALD
T21 1391-1412 SpecificDisease:D000326 denotes adrenomyeloneuropathy
T22 1464-1467 SpecificDisease:D000326 denotes AMN
T23 1506-1509 SpecificDisease:D000326 denotes ALD
T24 1544-1561 SpecificDisease:D000224 denotes Addison's disease

ncbi-valid

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 64-81 SpecificDisease denotes Addison's disease
T3 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T4 143-146 SpecificDisease denotes ALD
T5 153-168 DiseaseClass denotes genetic disease
T6 185-228 DiseaseClass denotes demyelination of the central nervous system
T7 230-251 DiseaseClass denotes adrenal insufficiency
T8 328-331 SpecificDisease denotes ALD
T9 474-477 SpecificDisease denotes ALD
T10 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T11 567-570 SpecificDisease denotes AMN
T12 642-663 DiseaseClass denotes Adrenal insufficiency
T13 665-682 SpecificDisease denotes Addison's disease
T14 714-717 SpecificDisease denotes AMN
T15 721-733 SpecificDisease denotes cerebral ALD
T16 781-784 SpecificDisease denotes ALD
T17 818-821 SpecificDisease denotes ALD
T18 840-857 SpecificDisease denotes Addison's disease
T19 1080-1108 DiseaseClass denotes adrenocortical insufficiency
T20 1369-1381 SpecificDisease denotes cerebral ALD
T21 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T22 1464-1467 SpecificDisease denotes AMN
T23 1506-1509 SpecificDisease denotes ALD
T24 1544-1561 SpecificDisease denotes Addison's disease

ncbi-valid-gpt-r-g

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 64-81 SpecificDisease denotes Addison's disease
T3 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T4 143-146 SpecificDisease denotes ALD
T5 153-168 DiseaseClass denotes genetic disease
T6 230-251 DiseaseClass denotes adrenal insufficiency
T7 328-331 SpecificDisease denotes ALD
T8 474-477 SpecificDisease denotes ALD
T9 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T10 567-570 SpecificDisease denotes AMN
T11 642-663 DiseaseClass denotes Adrenal insufficiency
T12 665-682 SpecificDisease denotes Addison's disease
T13 714-733 CompositeMention denotes AMN or cerebral ALD
T14 781-784 SpecificDisease denotes ALD
T15 840-857 SpecificDisease denotes Addison's disease
T16 1080-1108 DiseaseClass denotes adrenocortical insufficiency
T17 1369-1381 SpecificDisease denotes cerebral ALD
T18 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T19 1464-1467 SpecificDisease denotes AMN
T20 1506-1509 SpecificDisease denotes ALD
T21 1544-1561 SpecificDisease denotes Addison's disease

ncbi-valid-gpt-r-ng

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 53-63 Modifier denotes idiopathic
T3 64-81 SpecificDisease denotes Addison's disease
T4 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T5 143-146 SpecificDisease denotes ALD
T6 153-168 DiseaseClass denotes genetic disease
T7 230-251 DiseaseClass denotes adrenal insufficiency
T8 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T9 567-570 SpecificDisease denotes AMN
T10 642-663 DiseaseClass denotes Adrenal insufficiency
T11 665-682 SpecificDisease denotes Addison's disease
T12 721-733 CompositeMention denotes cerebral ALD
T13 1061-1068 Modifier denotes primary
T14 1069-1079 Modifier denotes idiopathic
T15 1080-1108 DiseaseClass denotes adrenocortical insufficiency
T16 1391-1438 CompositeMention denotes adrenomyeloneuropathy with cerebral involvement
T17 1452-1467 CompositeMention denotes preclinical AMN
T18 1533-1543 Modifier denotes idiopathic

ncbi-valid-gpt-nr-ng

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 53-63 Modifier denotes idiopathic
T3 64-81 SpecificDisease denotes Addison's disease
T4 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T5 143-146 SpecificDisease denotes ALD
T6 153-168 DiseaseClass denotes genetic disease
T7 230-251 SpecificDisease denotes adrenal insufficiency

ncbi-valid-gpt-nr-g

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 64-81 SpecificDisease denotes Addison's disease
T3 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T4 153-168 DiseaseClass denotes genetic disease

ncbi-valid-gemini-nr-ng

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 53-73 CompositeMention denotes idiopathic Addison's
T3 74-81 DiseaseClass denotes disease
T4 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T5 143-146 SpecificDisease denotes ALD
T6 153-168 DiseaseClass denotes genetic disease
T7 185-228 SpecificDisease denotes demyelination of the central nervous system
T8 230-251 SpecificDisease denotes adrenal insufficiency
T9 328-331 SpecificDisease denotes ALD
T10 474-477 SpecificDisease denotes ALD
T11 485-498 Modifier denotes cerebral form
T12 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T13 567-570 SpecificDisease denotes AMN
T14 642-663 SpecificDisease denotes Adrenal insufficiency
T15 665-682 SpecificDisease denotes Addison's disease
T16 721-733 CompositeMention denotes cerebral ALD
T17 818-821 SpecificDisease denotes ALD
T18 1061-1108 CompositeMention denotes primary idiopathic adrenocortical insufficiency
T19 1241-1266 SpecificDisease denotes adrenocortical antibodies
T20 1369-1381 CompositeMention denotes cerebral ALD
T21 1391-1438 SpecificDisease denotes adrenomyeloneuropathy with cerebral involvement
T22 1452-1467 CompositeMention denotes preclinical AMN
T23 1533-1553 CompositeMention denotes idiopathic Addison's
T24 1554-1561 DiseaseClass denotes disease

ncbi-valid-gemini-nr-g

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 53-81 SpecificDisease denotes idiopathic Addison's disease
T3 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T4 143-146 SpecificDisease denotes ALD
T5 153-168 DiseaseClass denotes genetic disease
T6 230-251 SpecificDisease denotes adrenal insufficiency
T7 328-331 SpecificDisease denotes ALD
T8 474-477 SpecificDisease denotes ALD
T9 485-498 SpecificDisease denotes cerebral form
T10 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T11 567-570 SpecificDisease denotes AMN
T12 642-663 SpecificDisease denotes Adrenal insufficiency
T13 665-682 SpecificDisease denotes Addison's disease
T14 721-733 SpecificDisease denotes cerebral ALD
T15 1061-1108 SpecificDisease denotes primary idiopathic adrenocortical insufficiency
T16 1378-1381 SpecificDisease denotes ALD
T17 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T18 1452-1467 SpecificDisease denotes preclinical AMN
T19 1533-1561 SpecificDisease denotes idiopathic Addison's disease

ncbi-valid-gemini-r-g

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 53-81 SpecificDisease denotes idiopathic Addison's disease
T3 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T4 143-146 SpecificDisease denotes ALD
T5 153-168 DiseaseClass denotes genetic disease
T6 185-228 DiseaseClass denotes demyelination of the central nervous system
T7 230-251 SpecificDisease denotes adrenal insufficiency
T8 328-331 SpecificDisease denotes ALD
T9 474-477 SpecificDisease denotes ALD
T10 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T11 567-570 SpecificDisease denotes AMN
T12 642-663 SpecificDisease denotes Adrenal insufficiency
T13 665-682 SpecificDisease denotes Addison's disease
T14 714-717 SpecificDisease denotes AMN
T15 721-733 SpecificDisease denotes cerebral ALD
T16 840-857 SpecificDisease denotes Addison's disease
T17 1061-1108 SpecificDisease denotes primary idiopathic adrenocortical insufficiency
T18 1369-1381 SpecificDisease denotes cerebral ALD
T19 1391-1438 SpecificDisease denotes adrenomyeloneuropathy with cerebral involvement
T20 1452-1467 SpecificDisease denotes preclinical AMN
T21 1533-1561 SpecificDisease denotes idiopathic Addison's disease

ncbi-valid-deepseek-nr-ng

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 30-32 Modifier denotes is
T3 33-43 Modifier denotes a frequent
T4 44-49 Modifier denotes cause
T5 50-63 Modifier denotes of idiopathic
T6 64-81 SpecificDisease denotes Addison's disease
T7 82-84 Modifier denotes in
T8 85-90 Modifier denotes young
T9 91-96 Modifier denotes adult
T10 97-101 Modifier denotes male
T11 102-110 Modifier denotes patients
T12 110-111 Modifier denotes .
T13 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T14 142-147 CompositeMention denotes (ALD)
T15 148-150 Modifier denotes is
T16 153-160 Modifier denotes genetic
T17 161-168 DiseaseClass denotes disease
T18 169-179 Modifier denotes associated
T19 180-184 Modifier denotes with
T20 185-198 DiseaseClass denotes demyelination
T21 199-201 Modifier denotes of
T22 202-205 Modifier denotes the
T23 206-213 Modifier denotes central
T24 214-221 Modifier denotes nervous
T25 222-228 Modifier denotes system
T26 228-229 Modifier denotes ,
T27 230-251 SpecificDisease denotes adrenal insufficiency
T28 253-256 Modifier denotes and
T29 257-269 Modifier denotes accumulation
T30 270-272 Modifier denotes of
T31 273-277 Modifier denotes very
T32 278-282 Modifier denotes long
T33 283-288 Modifier denotes chain
T34 289-294 Modifier denotes fatty
T35 295-300 Modifier denotes acids
T36 304-310 Modifier denotes tissue
T37 311-314 Modifier denotes and
T38 315-319 Modifier denotes body
T39 320-326 Modifier denotes fluids
T40 326-327 Modifier denotes .
T41 328-331 CompositeMention denotes ALD
T42 332-334 Modifier denotes is
T43 335-338 Modifier denotes due
T44 339-341 Modifier denotes to
T45 342-350 Modifier denotes mutation
T46 351-353 Modifier denotes of
T47 356-360 Modifier denotes gene
T48 361-368 Modifier denotes located
T49 369-371 Modifier denotes in
T50 372-376 Modifier denotes Xq28
T51 377-381 Modifier denotes that
T52 382-389 Modifier denotes encodes
T53 392-403 Modifier denotes peroxisomal
T54 404-415 Modifier denotes transporter
T55 416-423 Modifier denotes protein
T56 424-426 Modifier denotes of
T57 427-434 Modifier denotes unknown
T58 435-443 Modifier denotes function
T59 443-444 Modifier denotes .
T60 445-448 Modifier denotes The
T61 449-453 Modifier denotes most
T62 454-460 Modifier denotes common
T63 461-470 Modifier denotes phenotype
T64 471-473 Modifier denotes of
T65 474-477 CompositeMention denotes ALD
T66 478-480 Modifier denotes is
T67 481-484 Modifier denotes the
T68 485-493 Modifier denotes cerebral
T69 494-498 Modifier denotes form
T70 499-504 CompositeMention denotes (45%)
T71 505-509 Modifier denotes that
T72 510-518 Modifier denotes develops
T73 519-521 Modifier denotes in
T74 522-526 Modifier denotes boys
T75 527-534 Modifier denotes between
T76 535-539 Modifier denotes 5-12
T77 540-542 Modifier denotes yr
T78 542-543 Modifier denotes .
T79 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T80 566-571 CompositeMention denotes (AMN)
T81 572-580 Modifier denotes involves
T82 581-584 Modifier denotes the
T83 585-596 Modifier denotes spinal cord
T84 597-600 Modifier denotes and
T85 601-611 Modifier denotes peripheral
T86 612-618 Modifier denotes nerves
T87 619-621 Modifier denotes in
T88 622-627 Modifier denotes young
T89 628-634 Modifier denotes adults
T90 635-640 CompositeMention denotes (35%)
T91 640-641 Modifier denotes .
T92 642-663 SpecificDisease denotes Adrenal insufficiency
T93 664-683 CompositeMention denotes (Addison's disease)
T94 687-697 Modifier denotes frequently
T95 698-708 Modifier denotes associated
T96 709-713 Modifier denotes with
T97 714-717 CompositeMention denotes AMN
T98 718-720 Modifier denotes or
T99 721-729 Modifier denotes cerebral
T100 730-733 CompositeMention denotes ALD
T101 734-737 Modifier denotes and
T102 738-741 Modifier denotes may
T103 742-748 Modifier denotes remain
T104 749-752 Modifier denotes the
T105 753-757 Modifier denotes only
T106 758-766 Modifier denotes clinical
T107 767-777 Modifier denotes expression
T108 778-780 Modifier denotes of
T109 781-784 CompositeMention denotes ALD
T110 785-798 CompositeMention denotes (8% of cases)
T111 798-799 Modifier denotes .
T112 800-803 Modifier denotes The
T113 804-814 Modifier denotes prevalence
T114 818-821 CompositeMention denotes ALD
T115 822-827 Modifier denotes among
T116 828-834 Modifier denotes adults
T117 835-839 Modifier denotes with
T118 840-857 SpecificDisease denotes Addison's disease
T119 858-865 Modifier denotes remains
T120 866-873 Modifier denotes unknown
T121 873-874 Modifier denotes .
T122 875-877 Modifier denotes To
T123 878-886 Modifier denotes evaluate
T124 887-891 Modifier denotes this
T125 892-902 Modifier denotes prevalence
T126 902-903 Modifier denotes ,
T127 904-906 Modifier denotes we
T128 907-916 Modifier denotes performed
T129 917-928 Modifier denotes biochemical
T130 929-937 Modifier denotes analysis
T131 938-940 Modifier denotes of
T132 941-945 Modifier denotes very
T133 946-950 Modifier denotes long
T134 951-956 Modifier denotes chain
T135 957-962 Modifier denotes fatty
T136 963-968 Modifier denotes acids
T137 969-971 Modifier denotes in
T138 972-974 Modifier denotes 14
T139 975-979 Modifier denotes male
T140 980-988 Modifier denotes patients
T141 989-1029 CompositeMention denotes (age ranging from 12-45 yr at diagnosis)
T142 1030-1040 Modifier denotes previously
T143 1041-1050 Modifier denotes diagnosed
T144 1051-1053 Modifier denotes as
T145 1054-1060 Modifier denotes having
T146 1061-1068 Modifier denotes primary
T147 1069-1079 Modifier denotes idiopathic
T148 1080-1108 SpecificDisease denotes adrenocortical insufficiency
T149 1108-1109 Modifier denotes .
T150 1110-1112 Modifier denotes In
T151 1113-1114 Modifier denotes 5
T152 1115-1117 Modifier denotes of
T153 1118-1120 Modifier denotes 14
T154 1121-1129 Modifier denotes patients
T155 1130-1135 CompositeMention denotes (35%)
T156 1135-1136 Modifier denotes ,
T157 1137-1145 Modifier denotes elevated
T158 1146-1152 Modifier denotes plasma
T159 1153-1167 Modifier denotes concentrations
T160 1171-1175 Modifier denotes very
T161 1176-1180 Modifier denotes long
T162 1181-1186 Modifier denotes chain
T163 1187-1192 Modifier denotes fatty
T164 1193-1198 Modifier denotes acids
T165 1199-1203 Modifier denotes were
T166 1204-1212 Modifier denotes detected
T167 1212-1213 Modifier denotes .
T168 1214-1218 Modifier denotes None
T169 1219-1221 Modifier denotes of
T170 1222-1227 Modifier denotes these
T171 1228-1236 Modifier denotes patients
T172 1237-1240 Modifier denotes had
T173 1241-1266 Modifier denotes adrenocortical antibodies
T174 1266-1267 Modifier denotes .
T175 1268-1270 Modifier denotes By
T176 1271-1291 Modifier denotes electrophysiological
T177 1292-1297 Modifier denotes tests
T178 1298-1301 Modifier denotes and
T179 1302-1320 Modifier denotes magnetic resonance
T180 1321-1328 Modifier denotes imaging
T181 1329-1331 Modifier denotes it
T182 1332-1335 Modifier denotes was
T183 1336-1346 Modifier denotes determined
T184 1347-1351 Modifier denotes that
T185 1352-1355 Modifier denotes two
T186 1356-1364 Modifier denotes patients
T187 1365-1368 Modifier denotes had
T188 1369-1377 Modifier denotes cerebral
T189 1378-1381 CompositeMention denotes ALD
T190 1381-1382 Modifier denotes ,
T191 1383-1386 Modifier denotes one
T192 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T193 1413-1417 Modifier denotes with
T194 1418-1426 Modifier denotes cerebral
T195 1427-1438 Modifier denotes involvement
T196 1438-1439 Modifier denotes ,
T197 1440-1443 Modifier denotes and
T198 1444-1447 Modifier denotes two
T199 1448-1451 Modifier denotes had
T200 1452-1463 Modifier denotes preclinical
T201 1464-1467 CompositeMention denotes AMN
T202 1467-1468 Modifier denotes .
T203 1469-1472 Modifier denotes Our
T204 1473-1477 Modifier denotes data
T205 1478-1485 Modifier denotes support
T206 1486-1489 Modifier denotes the
T207 1490-1500 Modifier denotes hypothesis
T208 1501-1505 Modifier denotes that
T209 1506-1509 CompositeMention denotes ALD
T210 1515-1523 Modifier denotes frequent
T211 1524-1529 Modifier denotes cause
T212 1530-1532 Modifier denotes of
T213 1533-1543 Modifier denotes idiopathic
T214 1544-1561 SpecificDisease denotes Addison's disease
T215 1562-1564 Modifier denotes in
T216 1565-1573 Modifier denotes children
T217 1574-1577 Modifier denotes and
T218 1578-1584 Modifier denotes adults
T219 1584-1585 Modifier denotes .

ncbi-valid-deepseek-nr-g

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 53-81 SpecificDisease denotes idiopathic Addison's disease
T3 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T4 143-146 SpecificDisease denotes ALD
T5 153-168 DiseaseClass denotes genetic disease
T6 328-331 SpecificDisease denotes ALD
T7 485-493 Modifier denotes cerebral
T8 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T9 567-570 SpecificDisease denotes AMN
T10 642-663 SpecificDisease denotes Adrenal insufficiency
T11 665-682 SpecificDisease denotes Addison's disease
T12 714-717 SpecificDisease denotes AMN
T13 721-733 CompositeMention denotes cerebral ALD
T14 818-821 SpecificDisease denotes ALD
T15 1369-1381 CompositeMention denotes cerebral ALD
T16 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T17 1452-1467 CompositeMention denotes preclinical AMN
T18 1533-1561 SpecificDisease denotes idiopathic Addison's disease

ncbi-valid-deepseek-r-g

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 53-81 SpecificDisease denotes idiopathic Addison's disease
T3 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T4 143-146 SpecificDisease denotes ALD
T5 230-251 SpecificDisease denotes adrenal insufficiency
T6 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T7 567-570 SpecificDisease denotes AMN
T8 665-682 SpecificDisease denotes Addison's disease
T9 721-733 SpecificDisease denotes cerebral ALD
T10 1061-1108 SpecificDisease denotes primary idiopathic adrenocortical insufficiency
T11 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T12 1452-1467 SpecificDisease denotes preclinical AMN
T13 1533-1561 SpecificDisease denotes idiopathic Addison's disease

ncbi-valid-deepseek-r-ng

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 53-63 Modifier denotes idiopathic
T3 64-81 SpecificDisease denotes Addison's disease
T4 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T5 143-146 SpecificDisease denotes ALD
T6 153-168 DiseaseClass denotes genetic disease
T7 230-251 SpecificDisease denotes adrenal insufficiency
T8 485-493 Modifier denotes cerebral
T9 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T10 567-570 SpecificDisease denotes AMN
T11 665-682 SpecificDisease denotes Addison's disease
T12 721-733 CompositeMention denotes cerebral ALD
T13 1061-1108 CompositeMention denotes primary idiopathic adrenocortical insufficiency
T14 1391-1438 CompositeMention denotes adrenomyeloneuropathy with cerebral involvement
T15 1452-1467 CompositeMention denotes preclinical AMN
T16 1533-1561 CompositeMention denotes idiopathic Addison's disease

ncbi-valid-gemini-r-ng

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 53-63 Modifier denotes idiopathic
T3 64-81 SpecificDisease denotes Addison's disease
T4 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T5 143-146 SpecificDisease denotes ALD
T6 153-168 DiseaseClass denotes genetic disease
T7 185-228 SpecificDisease denotes demyelination of the central nervous system
T8 230-251 SpecificDisease denotes adrenal insufficiency
T9 257-326 SpecificDisease denotes accumulation of very long chain fatty acids in tissue and body fluids
T10 328-331 SpecificDisease denotes ALD
T11 474-477 SpecificDisease denotes ALD
T12 485-493 Modifier denotes cerebral
T13 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T14 567-570 SpecificDisease denotes AMN
T15 642-663 SpecificDisease denotes Adrenal insufficiency
T16 665-682 SpecificDisease denotes Addison's disease
T17 721-729 Modifier denotes cerebral
T18 730-733 SpecificDisease denotes ALD
T19 818-821 SpecificDisease denotes ALD
T20 1061-1068 Modifier denotes primary
T21 1069-1079 Modifier denotes idiopathic
T22 1080-1108 SpecificDisease denotes adrenocortical insufficiency
T23 1369-1377 Modifier denotes cerebral
T24 1378-1381 SpecificDisease denotes ALD
T25 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T26 1452-1463 Modifier denotes preclinical
T27 1464-1467 SpecificDisease denotes AMN
T28 1544-1561 SpecificDisease denotes Addison's disease

ncbi-valid-gemini-r-m

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 53-81 SpecificDisease denotes idiopathic Addison's disease
T3 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T4 143-146 SpecificDisease denotes ALD
T5 153-168 DiseaseClass denotes genetic disease
T6 230-251 SpecificDisease denotes adrenal insufficiency
T7 328-331 SpecificDisease denotes ALD
T8 474-477 SpecificDisease denotes ALD
T9 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T10 567-570 SpecificDisease denotes AMN
T11 642-663 SpecificDisease denotes Adrenal insufficiency
T12 665-682 SpecificDisease denotes Addison's disease
T13 714-717 SpecificDisease denotes AMN
T14 721-733 SpecificDisease denotes cerebral ALD
T15 840-857 SpecificDisease denotes Addison's disease
T16 1061-1108 SpecificDisease denotes primary idiopathic adrenocortical insufficiency
T17 1369-1381 SpecificDisease denotes cerebral ALD
T18 1391-1438 SpecificDisease denotes adrenomyeloneuropathy with cerebral involvement
T19 1452-1467 SpecificDisease denotes preclinical AMN
T20 1533-1561 SpecificDisease denotes idiopathic Addison's disease

ncbi-valid-gpt-r-m

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 64-81 SpecificDisease denotes Addison's disease
T3 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T4 143-146 SpecificDisease denotes ALD
T5 153-168 DiseaseClass denotes genetic disease
T6 230-251 DiseaseClass denotes adrenal insufficiency
T7 328-331 SpecificDisease denotes ALD
T8 474-477 SpecificDisease denotes ALD
T9 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T10 567-570 SpecificDisease denotes AMN
T11 642-663 DiseaseClass denotes Adrenal insufficiency
T12 665-682 SpecificDisease denotes Addison's disease
T13 714-717 SpecificDisease denotes AMN
T14 721-733 SpecificDisease denotes cerebral ALD
T15 781-784 SpecificDisease denotes ALD
T16 840-857 SpecificDisease denotes Addison's disease
T17 1061-1108 DiseaseClass denotes primary idiopathic adrenocortical insufficiency
T18 1369-1381 SpecificDisease denotes cerebral ALD
T19 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T20 1464-1467 SpecificDisease denotes AMN
T21 1506-1509 SpecificDisease denotes ALD
T22 1544-1561 SpecificDisease denotes Addison's disease

ncbi-valid-deepseek-r-m

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T2 53-81 SpecificDisease denotes idiopathic Addison's disease
T3 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T4 143-146 SpecificDisease denotes ALD
T5 153-168 DiseaseClass denotes genetic disease
T6 230-251 SpecificDisease denotes adrenal insufficiency
T7 328-331 SpecificDisease denotes ALD
T8 474-477 SpecificDisease denotes ALD
T9 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T10 567-570 SpecificDisease denotes AMN
T11 642-663 SpecificDisease denotes Adrenal insufficiency
T12 665-682 SpecificDisease denotes Addison's disease
T13 721-733 SpecificDisease denotes cerebral ALD
T14 1061-1108 SpecificDisease denotes primary idiopathic adrenocortical insufficiency
T15 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T16 1452-1467 SpecificDisease denotes preclinical AMN
T17 1533-1561 SpecificDisease denotes idiopathic Addison's disease

NCBI-Disease-Develop

Id Subject Object Predicate Lexical cue database_id
T179 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy D000326
T180 64-81 SpecificDisease denotes Addison's disease D000224
T181 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy D000326
T182 143-146 SpecificDisease denotes ALD D000326
T183 153-168 DiseaseClass denotes genetic disease D030342
T184 185-228 DiseaseClass denotes demyelination of the central nervous system D020279
T185 230-251 DiseaseClass denotes adrenal insufficiency D000309
T186 328-331 SpecificDisease denotes ALD D000326
T187 474-477 SpecificDisease denotes ALD D000326
T188 544-565 SpecificDisease denotes Adrenomyeloneuropathy D000326
T189 567-570 SpecificDisease denotes AMN D000326
T190 642-663 DiseaseClass denotes Adrenal insufficiency D000309
T191 665-682 SpecificDisease denotes Addison's disease D000224
T192 714-717 SpecificDisease denotes AMN D000326
T193 721-733 SpecificDisease denotes cerebral ALD D000326
T194 781-784 SpecificDisease denotes ALD D000326
T195 818-821 SpecificDisease denotes ALD D000326
T196 840-857 SpecificDisease denotes Addison's disease D000224
T197 1080-1108 DiseaseClass denotes adrenocortical insufficiency D000224
T198 1369-1381 SpecificDisease denotes cerebral ALD D000326
T199 1391-1412 SpecificDisease denotes adrenomyeloneuropathy D000326
T200 1464-1467 SpecificDisease denotes AMN D000326
T201 1506-1509 SpecificDisease denotes ALD D000326
T202 1544-1561 SpecificDisease denotes Addison's disease D000224

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T179 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy D000326
T180 64-81 SpecificDisease denotes Addison's disease D000224
T181 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy D000326
T182 143-146 SpecificDisease denotes ALD D000326
T183 153-168 DiseaseClass denotes genetic disease D030342
T184 185-228 DiseaseClass denotes demyelination of the central nervous system D020279
T185 230-251 DiseaseClass denotes adrenal insufficiency D000309
T186 328-331 SpecificDisease denotes ALD D000326
T187 474-477 SpecificDisease denotes ALD D000326
T188 544-565 SpecificDisease denotes Adrenomyeloneuropathy D000326
T189 567-570 SpecificDisease denotes AMN D000326
T190 642-663 DiseaseClass denotes Adrenal insufficiency D000309
T191 665-682 SpecificDisease denotes Addison's disease D000224
T192 714-717 SpecificDisease denotes AMN D000326
T193 721-733 SpecificDisease denotes cerebral ALD D000326
T194 781-784 SpecificDisease denotes ALD D000326
T195 818-821 SpecificDisease denotes ALD D000326
T196 840-857 SpecificDisease denotes Addison's disease D000224
T197 1080-1108 DiseaseClass denotes adrenocortical insufficiency D000224
T198 1369-1381 SpecificDisease denotes cerebral ALD D000326
T199 1391-1412 SpecificDisease denotes adrenomyeloneuropathy D000326
T200 1464-1467 SpecificDisease denotes AMN D000326
T201 1506-1509 SpecificDisease denotes ALD D000326
T202 1544-1561 SpecificDisease denotes Addison's disease D000224

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 53-81 SpecificDisease denotes idiopathic Addison's disease
T2 112-141 SpecificDisease denotes X-Linked adrenoleukodystrophy
T3 143-146 SpecificDisease denotes ALD
T4 230-251 SpecificDisease denotes adrenal insufficiency
T5 328-331 SpecificDisease denotes ALD
T6 474-477 SpecificDisease denotes ALD
T7 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T8 567-570 SpecificDisease denotes AMN
T9 642-663 SpecificDisease denotes Adrenal insufficiency
T10 665-682 SpecificDisease denotes Addison's disease
T11 714-717 SpecificDisease denotes AMN
T12 730-733 SpecificDisease denotes ALD
T13 781-784 SpecificDisease denotes ALD
T14 818-821 SpecificDisease denotes ALD
T15 840-857 SpecificDisease denotes Addison's disease
T16 1080-1108 SpecificDisease denotes adrenocortical insufficiency
T17 1378-1381 SpecificDisease denotes ALD
T18 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T19 1464-1467 SpecificDisease denotes AMN
T20 1506-1509 SpecificDisease denotes ALD
T21 1544-1561 SpecificDisease denotes Addison's disease

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 9-29 SpecificDisease denotes adrenoleukodystrophy
T2 64-81 SpecificDisease denotes Addison's disease
T3 121-141 SpecificDisease denotes adrenoleukodystrophy
T4 143-146 SpecificDisease denotes ALD
T5 230-251 SpecificDisease denotes adrenal insufficiency
T6 328-331 SpecificDisease denotes ALD
T7 474-477 SpecificDisease denotes ALD
T8 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T9 567-570 SpecificDisease denotes AMN
T10 642-663 Modifier denotes Adrenal insufficiency
T11 665-682 Modifier denotes Addison's disease
T12 714-717 SpecificDisease denotes AMN
T13 730-733 SpecificDisease denotes ALD
T14 781-784 SpecificDisease denotes ALD
T15 818-821 SpecificDisease denotes ALD
T16 840-857 Modifier denotes Addison's disease
T17 1080-1108 Modifier denotes adrenocortical insufficiency
T18 1378-1381 SpecificDisease denotes ALD
T19 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T20 1464-1467 SpecificDisease denotes AMN
T21 1506-1509 SpecificDisease denotes ALD
T22 1544-1561 SpecificDisease denotes Addison's disease

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 9-29 SpecificDisease denotes adrenoleukodystrophy
T2 64-81 SpecificDisease denotes Addison's disease
T3 121-141 SpecificDisease denotes adrenoleukodystrophy
T4 161-168 DiseaseClass denotes disease
T5 230-251 Modifier denotes adrenal insufficiency
T6 485-498 SpecificDisease denotes cerebral form
T7 544-565 SpecificDisease denotes Adrenomyeloneuropathy
T8 642-663 Modifier denotes Adrenal insufficiency
T9 665-682 SpecificDisease denotes Addison's disease
T10 840-857 SpecificDisease denotes Addison's disease
T11 1080-1108 Modifier denotes adrenocortical insufficiency
T12 1369-1381 SpecificDisease denotes cerebral ALD
T13 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T14 1418-1426 Modifier denotes cerebral
T15 1544-1561 SpecificDisease denotes Addison's disease

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease denotes X-linked adrenoleukodystrophy
T3 112-147 SpecificDisease denotes X-Linked adrenoleukodystrophy (ALD)
T4 230-237 Modifier denotes adrenal
T5 328-331 SpecificDisease denotes ALD
T6 474-477 SpecificDisease denotes ALD
T7 485-493 Modifier denotes cerebral
T8 544-571 SpecificDisease denotes Adrenomyeloneuropathy (AMN)
T9 619-649 CompositeMention denotes in young adults (35%). Adrenal
T10 665-682 SpecificDisease denotes Addison's disease
T11 714-717 SpecificDisease denotes AMN
T12 721-729 Modifier denotes cerebral
T13 730-733 SpecificDisease denotes ALD
T14 781-784 SpecificDisease denotes ALD
T15 818-821 SpecificDisease denotes ALD
T16 840-857 SpecificDisease denotes Addison's disease
T17 1069-1094 CompositeMention denotes idiopathic adrenocortical
T18 1241-1255 Modifier denotes adrenocortical
T19 1369-1377 Modifier denotes cerebral
T20 1378-1381 SpecificDisease denotes ALD
T21 1391-1412 SpecificDisease denotes adrenomyeloneuropathy
T22 1418-1426 Modifier denotes cerebral
T23 1464-1467 SpecificDisease denotes AMN
T24 1506-1509 SpecificDisease denotes ALD