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Id Subject Object Predicate Lexical cue
T7931 0-12 NN denotes Confirmation
T7932 13-15 IN denotes of
T7933 16-19 NN denotes QTL
T7934 20-22 NN denotes hg
T7935 19-20 HYPH denotes -
T7936 23-35 NNS denotes interactions
T7937 35-293 sentence denotes An important feature of our experimental design was the ability to test for interactions between QTL in each MMU2 donor region and genotype at the HG locus, since identical donor regions were introgressed on two genetic backgrounds, B6 (+/+) and HG (hg/hg).
T7938 36-38 DT denotes An
T7939 49-56 NN denotes feature
T7940 39-48 JJ denotes important
T7941 84-87 VBD denotes was
T7942 57-59 IN denotes of
T7943 60-63 PRP$ denotes our
T7944 77-83 NN denotes design
T7945 64-76 JJ denotes experimental
T7946 88-91 DT denotes the
T7947 92-99 NN denotes ability
T7948 100-102 TO denotes to
T7949 103-107 VB denotes test
T7950 108-111 IN denotes for
T7951 112-124 NNS denotes interactions
T7952 125-132 IN denotes between
T7953 133-136 NN denotes QTL
T7954 137-139 IN denotes in
T7955 140-144 DT denotes each
T7956 156-162 NN denotes region
T7957 145-149 NN denotes MMU2
T7958 150-155 NN denotes donor
T7959 163-166 CC denotes and
T7960 167-175 VB denotes genotype
T7961 176-178 IN denotes at
T7962 179-182 DT denotes the
T7963 186-191 NN denotes locus
T7964 183-185 NN denotes HG
T7965 191-193 , denotes ,
T7966 193-198 IN denotes since
T7967 228-240 VBN denotes introgressed
T7968 199-208 JJ denotes identical
T7969 215-222 NNS denotes regions
T7970 209-214 NN denotes donor
T7971 223-227 VBD denotes were
T7972 241-243 IN denotes on
T7973 244-247 CD denotes two
T7974 256-267 NNS denotes backgrounds
T7975 248-255 JJ denotes genetic
T7976 267-269 , denotes ,
T7977 269-271 NN denotes B6
T7978 272-273 -LRB- denotes (
T7979 275-276 SYM denotes +
T7980 273-274 SYM denotes +
T7981 274-275 HYPH denotes /
T7982 276-277 -RRB- denotes )
T7983 278-281 CC denotes and
T7984 282-284 NN denotes HG
T7985 285-286 -LRB- denotes (
T7986 289-291 NN denotes hg
T7987 286-288 NN denotes hg
T7988 288-289 HYPH denotes /
T7989 291-292 -RRB- denotes )
T7990 292-293 . denotes .
T7991 293-449 sentence denotes Significant interactions between donor region and HG genotype were viewed as strong evidence that hg modifier QTL reside within that unique genomic region.
T7992 294-305 JJ denotes Significant
T7993 306-318 NNS denotes interactions
T7994 361-367 VBN denotes viewed
T7995 319-326 IN denotes between
T7996 327-332 NN denotes donor
T7997 333-339 NN denotes region
T7998 340-343 CC denotes and
T7999 344-346 NN denotes HG
T8000 347-355 NN denotes genotype
T8001 356-360 VBD denotes were
T8002 368-370 IN denotes as
T8003 371-377 JJ denotes strong
T8004 378-386 NN denotes evidence
T8005 387-391 IN denotes that
T8006 408-414 VBP denotes reside
T8007 392-394 NN denotes hg
T8008 404-407 NN denotes QTL
T8009 395-403 NN denotes modifier
T8010 415-421 IN denotes within
T8011 422-426 DT denotes that
T8012 442-448 NN denotes region
T8013 427-433 JJ denotes unique
T8014 434-441 JJ denotes genomic
T8015 448-449 . denotes .
T8016 449-584 sentence denotes In the original linkage analysis the mode of gene action and peak location of Wg2 were dependent on the presence of hg [24] (Table 1).
T8017 450-452 IN denotes In
T8018 532-536 VBD denotes were
T8019 453-456 DT denotes the
T8020 474-482 NN denotes analysis
T8021 457-465 JJ denotes original
T8022 466-473 NN denotes linkage
T8023 483-486 DT denotes the
T8024 487-491 NN denotes mode
T8025 492-494 IN denotes of
T8026 495-499 NN denotes gene
T8027 500-506 NN denotes action
T8028 507-510 CC denotes and
T8029 511-515 JJ denotes peak
T8030 516-524 NN denotes location
T8031 525-527 IN denotes of
T8032 528-531 NN denotes Wg2
T8033 537-546 JJ denotes dependent
T8034 547-549 IN denotes on
T8035 550-553 DT denotes the
T8036 554-562 NN denotes presence
T8037 563-565 IN denotes of
T8038 566-568 NN denotes hg
T8039 569-570 -LRB- denotes [
T8040 570-572 CD denotes 24
T8041 572-573 -RRB- denotes ]
T8042 574-575 -LRB- denotes (
T8043 575-580 NN denotes Table
T8044 581-582 CD denotes 1
T8045 582-583 -RRB- denotes )
T8046 583-584 . denotes .
T8047 584-711 sentence denotes In the present study, only homozygous congenic mice were characterized, thus, the overdominant effects of Wg2 were not tested.
T8048 585-587 IN denotes In
T8049 704-710 VBN denotes tested
T8050 588-591 DT denotes the
T8051 600-605 NN denotes study
T8052 592-599 JJ denotes present
T8053 605-607 , denotes ,
T8054 607-611 RB denotes only
T8055 632-636 NNS denotes mice
T8056 612-622 JJ denotes homozygous
T8057 623-631 JJ denotes congenic
T8058 642-655 VBN denotes characterized
T8059 637-641 VBD denotes were
T8060 655-657 , denotes ,
T8061 657-661 RB denotes thus
T8062 661-663 , denotes ,
T8063 663-666 DT denotes the
T8064 680-687 NNS denotes effects
T8065 667-679 JJ denotes overdominant
T8066 688-690 IN denotes of
T8067 691-694 NN denotes Wg2
T8068 695-699 VBD denotes were
T8069 700-703 RB denotes not
T8070 710-711 . denotes .
T8071 711-952 sentence denotes However, since its original peak location differed dependent on background we hypothesized that Wg2 represents a set of linked QTL between 74.9 and 181.8 Mbp within the 2M and 2D donor regions (Region III–V), some of which interact with hg.
T8072 712-719 RB denotes However
T8073 790-802 VBD denotes hypothesized
T8074 719-721 , denotes ,
T8075 721-726 IN denotes since
T8076 754-762 VBD denotes differed
T8077 727-730 PRP$ denotes its
T8078 745-753 NN denotes location
T8079 731-739 JJ denotes original
T8080 740-744 NN denotes peak
T8081 763-772 RB denotes dependent
T8082 773-775 IN denotes on
T8083 776-786 NN denotes background
T8084 787-789 PRP denotes we
T8085 803-807 IN denotes that
T8086 812-822 VBZ denotes represents
T8087 808-811 NN denotes Wg2
T8088 823-824 DT denotes a
T8089 825-828 NN denotes set
T8090 829-831 IN denotes of
T8091 832-838 VBN denotes linked
T8092 839-842 NN denotes QTL
T8093 843-850 IN denotes between
T8094 851-855 CD denotes 74.9
T8095 866-869 NN denotes Mbp
T8096 856-859 CC denotes and
T8097 860-865 CD denotes 181.8
T8098 870-876 IN denotes within
T8099 877-880 DT denotes the
T8100 897-904 NNS denotes regions
T8101 881-883 NN denotes 2M
T8102 884-887 CC denotes and
T8103 888-890 NN denotes 2D
T8104 891-896 NN denotes donor
T8105 905-906 -LRB- denotes (
T8106 906-912 NN denotes Region
T8107 913-916 CD denotes III
T8108 916-917 SYM denotes –
T8109 917-918 CD denotes V
T8110 918-919 -RRB- denotes )
T8111 919-921 , denotes ,
T8112 921-925 DT denotes some
T8113 935-943 VBP denotes interact
T8114 926-928 IN denotes of
T8115 929-934 WDT denotes which
T8116 944-948 IN denotes with
T8117 949-951 NN denotes hg
T8118 951-952 . denotes .
T8119 952-1070 sentence denotes Following this logic we expected one or both of these strains would exhibit donor region by HG genotype interactions.
T8120 953-962 VBG denotes Following
T8121 977-985 VBD denotes expected
T8122 963-967 DT denotes this
T8123 968-973 NN denotes logic
T8124 974-976 PRP denotes we
T8125 986-989 CD denotes one
T8126 1021-1028 VB denotes exhibit
T8127 990-992 CC denotes or
T8128 993-997 DT denotes both
T8129 998-1000 IN denotes of
T8130 1001-1006 DT denotes these
T8131 1007-1014 NNS denotes strains
T8132 1015-1020 MD denotes would
T8133 1029-1034 NN denotes donor
T8134 1035-1041 NN denotes region
T8135 1057-1069 NNS denotes interactions
T8136 1042-1044 IN denotes by
T8137 1045-1047 NN denotes HG
T8138 1048-1056 NN denotes genotype
T8139 1069-1070 . denotes .
T8140 1070-1127 sentence denotes Unfortunately, we were unable to characterize HG2D mice.
T8141 1071-1084 RB denotes Unfortunately
T8142 1089-1093 VBD denotes were
T8143 1084-1086 , denotes ,
T8144 1086-1088 PRP denotes we
T8145 1094-1100 JJ denotes unable
T8146 1101-1103 TO denotes to
T8147 1104-1116 VB denotes characterize
T8148 1117-1121 NN denotes HG2D
T8149 1122-1126 NNS denotes mice
T8150 1126-1127 . denotes .
T8151 1127-1204 sentence denotes However, as noted above, strong sex-specific effects were seen in HG2M mice.
T8152 1128-1135 RB denotes However
T8153 1186-1190 VBN denotes seen
T8154 1135-1137 , denotes ,
T8155 1137-1139 IN denotes as
T8156 1140-1145 VBN denotes noted
T8157 1146-1151 RB denotes above
T8158 1151-1153 , denotes ,
T8159 1153-1159 JJ denotes strong
T8160 1173-1180 NNS denotes effects
T8161 1160-1163 NN denotes sex
T8162 1164-1172 JJ denotes specific
T8163 1163-1164 HYPH denotes -
T8164 1181-1185 VBD denotes were
T8165 1191-1193 IN denotes in
T8166 1194-1198 NN denotes HG2M
T8167 1199-1203 NNS denotes mice
T8168 1203-1204 . denotes .
T8169 1204-1341 sentence denotes Significant 2M donor region by HG genotype by sex three-way interactions for AI (P = 0.0004; Figure 4) and TF were identified (Table 3).
T8170 1205-1216 JJ denotes Significant
T8171 1265-1277 NNS denotes interactions
T8172 1217-1219 NN denotes 2M
T8173 1226-1232 NN denotes region
T8174 1220-1225 NN denotes donor
T8175 1233-1235 IN denotes by
T8176 1236-1238 NN denotes HG
T8177 1239-1247 NN denotes genotype
T8178 1248-1250 IN denotes by
T8179 1251-1254 NN denotes sex
T8180 1255-1260 CD denotes three
T8181 1261-1264 NN denotes way
T8182 1260-1261 HYPH denotes -
T8183 1320-1330 VBN denotes identified
T8184 1278-1281 IN denotes for
T8185 1282-1284 NN denotes AI
T8186 1285-1286 -LRB- denotes (
T8187 1298-1304 NN denotes Figure
T8188 1286-1287 NN denotes P
T8189 1290-1296 CD denotes 0.0004
T8190 1288-1289 SYM denotes =
T8191 1296-1297 : denotes ;
T8192 1305-1306 CD denotes 4
T8193 1306-1307 -RRB- denotes )
T8194 1308-1311 CC denotes and
T8195 1312-1314 NN denotes TF
T8196 1315-1319 VBD denotes were
T8197 1331-1332 -LRB- denotes (
T8198 1332-1337 NN denotes Table
T8199 1338-1339 CD denotes 3
T8200 1339-1340 -RRB- denotes )
T8201 1340-1341 . denotes .
T8202 1341-1502 sentence denotes The basis of these interactions was a decrease in HG2M female and an increase in HG2M male adiposity, with no differences in fat accumulation across B62M sexes.
T8203 1342-1345 DT denotes The
T8204 1346-1351 NN denotes basis
T8205 1374-1377 VBD denotes was
T8206 1352-1354 IN denotes of
T8207 1355-1360 DT denotes these
T8208 1361-1373 NNS denotes interactions
T8209 1378-1379 DT denotes a
T8210 1380-1388 NN denotes decrease
T8211 1389-1391 IN denotes in
T8212 1392-1396 NN denotes HG2M
T8213 1397-1403 NN denotes female
T8214 1404-1407 CC denotes and
T8215 1408-1410 DT denotes an
T8216 1411-1419 NN denotes increase
T8217 1433-1442 NN denotes adiposity
T8218 1420-1422 IN denotes in
T8219 1423-1427 NN denotes HG2M
T8220 1428-1432 JJ denotes male
T8221 1442-1444 , denotes ,
T8222 1444-1448 IN denotes with
T8223 1449-1451 DT denotes no
T8224 1452-1463 NNS denotes differences
T8225 1464-1466 IN denotes in
T8226 1467-1470 NN denotes fat
T8227 1471-1483 NN denotes accumulation
T8228 1484-1490 IN denotes across
T8229 1491-1495 NN denotes B62M
T8230 1496-1501 NNS denotes sexes
T8231 1501-1502 . denotes .
T8232 1502-1660 sentence denotes Significant 2PM donor region by HG genotype two-way and 2PM donor region by HG genotype by sex three-way interactions were also seen for TF and AI (Table 3).
T8233 1503-1514 JJ denotes Significant
T8234 1608-1620 NNS denotes interactions
T8235 1515-1518 NN denotes 2PM
T8236 1525-1531 NN denotes region
T8237 1519-1524 NN denotes donor
T8238 1551-1554 NN denotes way
T8239 1532-1534 IN denotes by
T8240 1535-1537 NN denotes HG
T8241 1538-1546 NN denotes genotype
T8242 1547-1550 CD denotes two
T8243 1550-1551 HYPH denotes -
T8244 1555-1558 CC denotes and
T8245 1559-1562 NN denotes 2PM
T8246 1569-1575 NN denotes region
T8247 1563-1568 NN denotes donor
T8248 1604-1607 NN denotes way
T8249 1576-1578 IN denotes by
T8250 1579-1581 NN denotes HG
T8251 1582-1590 NN denotes genotype
T8252 1591-1593 IN denotes by
T8253 1594-1597 NN denotes sex
T8254 1598-1603 CD denotes three
T8255 1603-1604 HYPH denotes -
T8256 1631-1635 VBN denotes seen
T8257 1621-1625 VBD denotes were
T8258 1626-1630 RB denotes also
T8259 1636-1639 IN denotes for
T8260 1640-1642 NN denotes TF
T8261 1643-1646 CC denotes and
T8262 1647-1649 NN denotes AI
T8263 1650-1651 -LRB- denotes (
T8264 1651-1656 NN denotes Table
T8265 1657-1658 CD denotes 3
T8266 1658-1659 -RRB- denotes )
T8267 1659-1660 . denotes .
T8268 1660-1849 sentence denotes In addition, significant 2P donor region × HG genotype interactions were observed for all traits listed, although some traits did reached significance at the critical P < 0.0071 (Table 3).
T8269 1661-1663 IN denotes In
T8270 1734-1742 VBN denotes observed
T8271 1664-1672 NN denotes addition
T8272 1672-1674 , denotes ,
T8273 1674-1685 JJ denotes significant
T8274 1716-1728 NNS denotes interactions
T8275 1686-1688 NN denotes 2P
T8276 1695-1701 NN denotes region
T8277 1689-1694 NN denotes donor
T8278 1702-1703 SYM denotes ×
T8279 1707-1715 NN denotes genotype
T8280 1704-1706 NN denotes HG
T8281 1729-1733 VBD denotes were
T8282 1743-1746 IN denotes for
T8283 1747-1750 DT denotes all
T8284 1751-1757 NNS denotes traits
T8285 1758-1764 VBN denotes listed
T8286 1764-1766 , denotes ,
T8287 1766-1774 IN denotes although
T8288 1791-1798 VBN denotes reached
T8289 1775-1779 DT denotes some
T8290 1780-1786 NNS denotes traits
T8291 1787-1790 VBD denotes did
T8292 1799-1811 NN denotes significance
T8293 1812-1814 IN denotes at
T8294 1815-1818 DT denotes the
T8295 1832-1838 CD denotes 0.0071
T8296 1819-1827 JJ denotes critical
T8297 1828-1829 NN denotes P
T8298 1830-1831 SYM denotes <
T8299 1839-1840 -LRB- denotes (
T8300 1840-1845 NN denotes Table
T8301 1846-1847 CD denotes 3
T8302 1847-1848 -RRB- denotes )
T8303 1848-1849 . denotes .
T8304 1849-1972 sentence denotes The basis for each interaction was a decrease in phenotype in HG2P compared to HGC and no difference between B62P and B6C.
T8305 1850-1853 DT denotes The
T8306 1854-1859 NN denotes basis
T8307 1881-1884 VBD denotes was
T8308 1860-1863 IN denotes for
T8309 1864-1868 DT denotes each
T8310 1869-1880 NN denotes interaction
T8311 1885-1886 DT denotes a
T8312 1887-1895 NN denotes decrease
T8313 1896-1898 IN denotes in
T8314 1899-1908 NN denotes phenotype
T8315 1909-1911 IN denotes in
T8316 1912-1916 NN denotes HG2P
T8317 1917-1925 VBN denotes compared
T8318 1926-1928 IN denotes to
T8319 1929-1932 NN denotes HGC
T8320 1933-1936 CC denotes and
T8321 1937-1939 DT denotes no
T8322 1940-1950 NN denotes difference
T8323 1951-1958 IN denotes between
T8324 1959-1963 NN denotes B62P
T8325 1964-1967 CC denotes and
T8326 1968-1971 NN denotes B6C
T8327 1971-1972 . denotes .
T8328 1972-2053 sentence denotes Together these data confirm that MMU2 QTL modify the effects of the hg deletion.
T8329 1973-1981 RB denotes Together
T8330 1993-2000 VBP denotes confirm
T8331 1982-1987 DT denotes these
T8332 1988-1992 NNS denotes data
T8333 2001-2005 IN denotes that
T8334 2015-2021 VBP denotes modify
T8335 2006-2010 NN denotes MMU2
T8336 2011-2014 NN denotes QTL
T8337 2022-2025 DT denotes the
T8338 2026-2033 NNS denotes effects
T8339 2034-2036 IN denotes of
T8340 2037-2040 DT denotes the
T8341 2044-2052 NN denotes deletion
T8342 2041-2043 NN denotes hg
T8343 2052-2053 . denotes .
R2289 T7983 T7977 cc and,B6
R2290 T7932 T7931 prep of,Confirmation
R2291 T7933 T7934 compound QTL,hg
R2292 T7934 T7936 compound hg,interactions
R2293 T7935 T7934 punct -,hg
R2294 T7984 T7977 conj HG,B6
R2295 T7936 T7932 pobj interactions,of
R2296 T7985 T7986 punct (,hg
R2297 T7938 T7939 det An,feature
R2298 T7939 T7941 nsubj feature,was
R2299 T7940 T7939 amod important,feature
R2300 T7986 T7984 parataxis hg,HG
R2301 T7942 T7939 prep of,feature
R2302 T7943 T7944 poss our,design
R2303 T7944 T7942 pobj design,of
R2304 T7945 T7944 amod experimental,design
R2305 T7946 T7947 det the,ability
R2306 T7987 T7986 compound hg,hg
R2307 T7947 T7941 attr ability,was
R2308 T7948 T7949 aux to,test
R2309 T7949 T7947 acl test,ability
R2310 T7988 T7986 punct /,hg
R2311 T7950 T7949 prep for,test
R2312 T7951 T7950 pobj interactions,for
R2313 T7952 T7951 prep between,interactions
R2314 T7989 T7986 punct ),hg
R2315 T7953 T7952 pobj QTL,between
R2316 T7954 T7949 prep in,test
R2317 T7990 T7941 punct .,was
R2318 T7955 T7956 det each,region
R2319 T7956 T7954 pobj region,in
R2320 T7957 T7958 compound MMU2,donor
R2321 T7958 T7956 compound donor,region
R2322 T7992 T7993 amod Significant,interactions
R2323 T7959 T7949 cc and,test
R2324 T7960 T7949 conj genotype,test
R2325 T7961 T7960 prep at,genotype
R2326 T7962 T7963 det the,locus
R2327 T7993 T7994 nsubjpass interactions,viewed
R2328 T7963 T7961 pobj locus,at
R2329 T7964 T7963 compound HG,locus
R2330 T7965 T7960 punct ", ",genotype
R2331 T7995 T7993 prep between,interactions
R2332 T7966 T7967 mark since,introgressed
R2333 T7996 T7997 compound donor,region
R2334 T7967 T7960 advcl introgressed,genotype
R2335 T7968 T7969 amod identical,regions
R2336 T7997 T7995 pobj region,between
R2337 T7969 T7967 nsubjpass regions,introgressed
R2338 T7970 T7969 compound donor,regions
R2339 T7971 T7967 auxpass were,introgressed
R2340 T7998 T7997 cc and,region
R2341 T7972 T7967 prep on,introgressed
R2342 T7973 T7974 nummod two,backgrounds
R2343 T7974 T7972 pobj backgrounds,on
R2345 T7975 T7974 amod genetic,backgrounds
R2346 T7976 T7974 punct ", ",backgrounds
R2347 T8000 T7997 conj genotype,region
R2348 T7977 T7974 appos B6,backgrounds
R2349 T7978 T7979 punct (,+
R2350 T8001 T7994 auxpass were,viewed
R2351 T7979 T7977 punct +,B6
R2352 T7980 T7979 punct +,+
R2353 T8002 T7994 prep as,viewed
R2354 T7981 T7979 punct /,+
R2355 T7982 T7979 punct ),+
R2356 T8003 T8004 amod strong,evidence
R2357 T8004 T8002 pobj evidence,as
R2358 T8089 T8086 dobj set,represents
R2359 T8005 T8006 mark that,reside
R2360 T8090 T8089 prep of,set
R2361 T8091 T8092 amod linked,QTL
R2362 T8092 T8090 pobj QTL,of
R2363 T8006 T8004 acl reside,evidence
R2364 T8093 T8092 prep between,QTL
R2365 T8094 T8095 nummod 74.9,Mbp
R2366 T8095 T8093 pobj Mbp,between
R2367 T8096 T8094 cc and,74.9
R2368 T8007 T8008 compound hg,QTL
R2369 T8097 T8094 conj 181.8,74.9
R2370 T8098 T8089 prep within,set
R2371 T8008 T8006 nsubj QTL,reside
R2372 T8099 T8100 det the,regions
R2373 T8100 T8098 pobj regions,within
R2374 T8101 T8100 nmod 2M,regions
R2375 T8009 T8008 compound modifier,QTL
R2376 T8102 T8101 cc and,2M
R2377 T8103 T8101 conj 2D,2M
R2378 T8104 T8100 compound donor,regions
R2379 T8010 T8006 prep within,reside
R2380 T8105 T8100 punct (,regions
R2381 T8106 T8107 nmod Region,III
R2382 T8107 T8100 appos III,regions
R2383 T8011 T8012 det that,region
R2384 T8108 T8109 punct –,V
R2385 T8109 T8107 prep V,III
R2386 T8110 T8100 punct ),regions
R2387 T8012 T8010 pobj region,within
R2388 T8111 T8100 punct ", ",regions
R2389 T8112 T8113 dep some,interact
R2390 T8113 T8100 relcl interact,regions
R2391 T8013 T8012 amod unique,region
R2392 T8114 T8112 prep of,some
R2393 T8115 T8114 pobj which,of
R2394 T8116 T8113 prep with,interact
R2395 T8014 T8012 amod genomic,region
R2396 T8117 T8116 pobj hg,with
R2397 T8118 T8073 punct .,hypothesized
R2398 T8015 T7994 punct .,viewed
R2399 T8120 T8121 advcl Following,expected
R2400 T8122 T8123 det this,logic
R2401 T8017 T8018 prep In,were
R2402 T8123 T8120 dobj logic,Following
R2403 T8124 T8121 nsubj we,expected
R2404 T8125 T8126 nsubj one,exhibit
R2405 T8126 T8121 advcl exhibit,expected
R2406 T8127 T8125 cc or,one
R2407 T8128 T8125 conj both,one
R2408 T8129 T8125 prep of,one
R2409 T8019 T8020 det the,analysis
R2410 T8130 T8131 det these,strains
R2411 T8131 T8129 pobj strains,of
R2412 T8132 T8126 aux would,exhibit
R2413 T8133 T8134 nmod donor,region
R2414 T8134 T8135 nmod region,interactions
R2415 T8020 T8017 pobj analysis,In
R2416 T8135 T8126 dobj interactions,exhibit
R2417 T8136 T8134 prep by,region
R2418 T8137 T8138 compound HG,genotype
R2419 T8021 T8020 amod original,analysis
R2420 T8138 T8136 pobj genotype,by
R2421 T8022 T8020 compound linkage,analysis
R2422 T8139 T8121 punct .,expected
R2423 T8023 T8024 det the,mode
R2424 T8141 T8142 advmod Unfortunately,were
R2425 T8024 T8018 nsubj mode,were
R2426 T8143 T8142 punct ", ",were
R2427 T8144 T8142 nsubj we,were
R2428 T8025 T8024 prep of,mode
R2429 T8145 T8142 acomp unable,were
R2430 T8146 T8147 aux to,characterize
R2431 T8147 T8145 xcomp characterize,unable
R2432 T8026 T8027 compound gene,action
R2433 T8148 T8149 compound HG2D,mice
R2434 T8149 T8147 dobj mice,characterize
R2435 T8027 T8025 pobj action,of
R2436 T8150 T8142 punct .,were
R2437 T8152 T8153 advmod However,seen
R2438 T8028 T8024 cc and,mode
R2439 T8154 T8153 punct ", ",seen
R2440 T8155 T8156 mark as,noted
R2441 T8029 T8030 amod peak,location
R2442 T8156 T8153 advcl noted,seen
R2443 T8157 T8156 advmod above,noted
R2444 T8158 T8153 punct ", ",seen
R2445 T8030 T8024 conj location,mode
R2446 T8159 T8160 amod strong,effects
R2447 T8160 T8153 nsubjpass effects,seen
R2448 T8161 T8162 npadvmod sex,specific
R2449 T8031 T8030 prep of,location
R2450 T8162 T8160 amod specific,effects
R2451 T8163 T8162 punct -,specific
R2452 T8032 T8031 pobj Wg2,of
R2453 T8164 T8153 auxpass were,seen
R2454 T8165 T8153 prep in,seen
R2455 T8166 T8167 compound HG2M,mice
R2456 T8033 T8018 acomp dependent,were
R2457 T8167 T8165 pobj mice,in
R2458 T8168 T8153 punct .,seen
R2459 T8170 T8171 amod Significant,interactions
R2460 T8171 T8183 nsubjpass interactions,identified
R2461 T8172 T8173 nmod 2M,region
R2462 T8034 T8033 prep on,dependent
R2463 T8173 T8171 nmod region,interactions
R2464 T8174 T8173 nmod donor,region
R2465 T8035 T8036 det the,presence
R2466 T8175 T8173 prep by,region
R2467 T8036 T8034 pobj presence,on
R2468 T8176 T8177 compound HG,genotype
R2469 T8177 T8175 pobj genotype,by
R2470 T8037 T8036 prep of,presence
R2471 T8178 T8173 prep by,region
R2472 T8179 T8178 pobj sex,by
R2473 T8180 T8181 nummod three,way
R2474 T8038 T8037 pobj hg,of
R2475 T8181 T8171 compound way,interactions
R2476 T8182 T8181 punct -,way
R2477 T8039 T8040 punct [,24
R2478 T8184 T8171 prep for,interactions
R2479 T8185 T8184 pobj AI,for
R2480 T8040 T8018 parataxis 24,were
R2481 T8186 T8187 punct (,Figure
R2482 T8187 T8185 parataxis Figure,AI
R2483 T8188 T8189 nsubj P,0.0004
R2484 T8041 T8040 punct ],24
R2485 T8189 T8187 ccomp 0.0004,Figure
R2486 T8190 T8189 punct =,0.0004
R2487 T8191 T8187 punct ;,Figure
R2488 T8042 T8043 punct (,Table
R2489 T8192 T8187 nummod 4,Figure
R2490 T8193 T8187 punct ),Figure
R2491 T8194 T8185 cc and,AI
R2492 T8043 T8018 parataxis Table,were
R2493 T8044 T8043 nummod 1,Table
R2494 T8045 T8043 punct ),Table
R2495 T8195 T8185 conj TF,AI
R2496 T8046 T8018 punct .,were
R2497 T8196 T8183 auxpass were,identified
R2498 T8197 T8198 punct (,Table
R2499 T8048 T8049 prep In,tested
R2500 T8198 T8183 parataxis Table,identified
R2501 T8199 T8198 nummod 3,Table
R2502 T8200 T8198 punct ),Table
R2503 T8201 T8183 punct .,identified
R2504 T8050 T8051 det the,study
R2505 T8203 T8204 det The,basis
R2506 T8204 T8205 nsubj basis,was
R2507 T8051 T8048 pobj study,In
R2508 T8206 T8204 prep of,basis
R2509 T8207 T8208 det these,interactions
R2510 T8208 T8206 pobj interactions,of
R2511 T8209 T8210 det a,decrease
R2512 T8052 T8051 amod present,study
R2513 T8210 T8205 attr decrease,was
R2514 T8211 T8210 prep in,decrease
R2515 T8212 T8213 compound HG2M,female
R2516 T8213 T8211 pobj female,in
R2517 T8053 T8049 punct ", ",tested
R2518 T8214 T8210 cc and,decrease
R2519 T8215 T8216 det an,increase
R2520 T8216 T8217 nmod increase,adiposity
R2521 T8054 T8055 advmod only,mice
R2522 T8217 T8210 conj adiposity,decrease
R2523 T8218 T8216 prep in,increase
R2524 T8219 T8218 pobj HG2M,in
R2525 T8055 T8058 nsubjpass mice,characterized
R2526 T8220 T8219 amod male,HG2M
R2527 T8221 T8210 punct ", ",decrease
R2528 T8222 T8210 prep with,decrease
R2529 T8056 T8055 amod homozygous,mice
R2530 T8223 T8224 det no,differences
R2531 T8224 T8222 pobj differences,with
R2532 T8225 T8224 prep in,differences
R2533 T8057 T8055 amod congenic,mice
R2534 T8226 T8227 compound fat,accumulation
R2535 T8227 T8225 pobj accumulation,in
R2536 T8058 T8049 ccomp characterized,tested
R2537 T8228 T8224 prep across,differences
R2538 T8059 T8058 auxpass were,characterized
R2539 T8229 T8230 compound B62M,sexes
R2540 T8230 T8228 pobj sexes,across
R2541 T8060 T8049 punct ", ",tested
R2542 T8231 T8205 punct .,was
R2543 T8233 T8234 amod Significant,interactions
R2544 T8061 T8049 advmod thus,tested
R2545 T8234 T8256 nsubjpass interactions,seen
R2546 T8235 T8236 nmod 2PM,region
R2547 T8236 T8238 nmod region,way
R2548 T8062 T8049 punct ", ",tested
R2549 T8237 T8236 nmod donor,region
R2550 T8238 T8234 nmod way,interactions
R2551 T8239 T8236 prep by,region
R2552 T8063 T8064 det the,effects
R2553 T8240 T8241 compound HG,genotype
R2554 T8241 T8239 pobj genotype,by
R2555 T8064 T8049 nsubjpass effects,tested
R2556 T8242 T8238 nummod two,way
R2557 T8243 T8238 punct -,way
R2558 T8244 T8238 cc and,way
R2559 T8065 T8064 amod overdominant,effects
R2560 T8245 T8246 nmod 2PM,region
R2561 T8246 T8248 nmod region,way
R2562 T8247 T8246 nmod donor,region
R2563 T8248 T8238 conj way,way
R2564 T8249 T8246 prep by,region
R2565 T8250 T8251 compound HG,genotype
R2566 T8066 T8064 prep of,effects
R2567 T8251 T8249 pobj genotype,by
R2568 T8252 T8246 prep by,region
R2569 T8253 T8252 pobj sex,by
R2570 T8067 T8066 pobj Wg2,of
R2571 T8254 T8248 nummod three,way
R2572 T8255 T8248 punct -,way
R2573 T8068 T8049 auxpass were,tested
R2574 T8257 T8256 auxpass were,seen
R2575 T8258 T8256 advmod also,seen
R2576 T8069 T8049 neg not,tested
R2577 T8259 T8256 prep for,seen
R2578 T8260 T8259 pobj TF,for
R2579 T8261 T8260 cc and,TF
R2580 T8070 T8049 punct .,tested
R2581 T8262 T8260 conj AI,TF
R2582 T8263 T8264 punct (,Table
R2583 T8264 T8256 parataxis Table,seen
R2584 T8072 T8073 advmod However,hypothesized
R2585 T8265 T8264 nummod 3,Table
R2586 T8266 T8264 punct ),Table
R2587 T8267 T8256 punct .,seen
R2588 T8074 T8073 punct ", ",hypothesized
R2589 T8269 T8270 prep In,observed
R2590 T8271 T8269 pobj addition,In
R2591 T8272 T8270 punct ", ",observed
R2592 T8075 T8076 mark since,differed
R2593 T8273 T8274 amod significant,interactions
R2594 T8274 T8270 nsubjpass interactions,observed
R2595 T8076 T8073 advcl differed,hypothesized
R2596 T8275 T8276 nmod 2P,region
R2597 T8276 T8274 nmod region,interactions
R2598 T8277 T8276 nmod donor,region
R2599 T8077 T8078 poss its,location
R2600 T8278 T8279 punct ×,genotype
R2601 T8279 T8276 prep genotype,region
R2602 T8280 T8279 compound HG,genotype
R2603 T8078 T8076 nsubj location,differed
R2604 T8281 T8270 auxpass were,observed
R2605 T8282 T8270 prep for,observed
R2606 T8283 T8284 det all,traits
R2607 T8079 T8078 amod original,location
R2608 T8284 T8282 pobj traits,for
R2609 T8285 T8284 acl listed,traits
R2610 T8286 T8270 punct ", ",observed
R2611 T8080 T8078 compound peak,location
R2613 T8288 T8270 advcl reached,observed
R2614 T8289 T8290 det some,traits
R2615 T8290 T8288 nsubj traits,reached
R2616 T8291 T8288 aux did,reached
R2618 T8081 T8076 advcl dependent,differed
R2619 T8293 T8288 prep at,reached
R2620 T8294 T8295 det the,0.0071
R2621 T8295 T8293 pobj 0.0071,at
R2622 T8082 T8081 prep on,dependent
R2623 T8296 T8295 amod critical,0.0071
R2624 T8297 T8295 nsubj P,0.0071
R2625 T8298 T8295 punct <,0.0071
R2626 T8083 T8082 pobj background,on
R2627 T8299 T8300 punct (,Table
R2628 T8300 T8270 parataxis Table,observed
R2629 T8084 T8073 nsubj we,hypothesized
R2630 T8085 T8086 mark that,represents
R2631 T8086 T8073 ccomp represents,hypothesized
R2632 T8301 T8300 nummod 3,Table
R2633 T8302 T8300 punct ),Table
R2634 T8087 T8086 nsubj Wg2,represents
R2635 T8303 T8270 punct .,observed
R2636 T8088 T8089 det a,set
R2637 T8305 T8306 det The,basis
R2638 T8306 T8307 nsubj basis,was
R2639 T8308 T8306 prep for,basis
R2640 T8309 T8310 det each,interaction
R2641 T8310 T8308 pobj interaction,for
R2642 T8311 T8312 det a,decrease
R2643 T8312 T8307 attr decrease,was
R2644 T8313 T8312 prep in,decrease
R2645 T8314 T8313 pobj phenotype,in
R2646 T8315 T8312 prep in,decrease
R2647 T8316 T8315 pobj HG2P,in
R2648 T8317 T8312 prep compared,decrease
R2649 T8318 T8317 prep to,compared
R2650 T8319 T8318 pobj HGC,to
R2651 T8320 T8312 cc and,decrease
R2652 T8321 T8322 det no,difference
R2653 T8322 T8312 conj difference,decrease
R2654 T8323 T8322 prep between,difference
R2655 T8324 T8323 pobj B62P,between
R2656 T8325 T8324 cc and,B62P
R2657 T8326 T8324 conj B6C,B62P
R2658 T8327 T8307 punct .,was
R2659 T8329 T8330 advmod Together,confirm
R2660 T8331 T8332 det these,data
R2661 T8332 T8330 nsubj data,confirm
R2662 T8333 T8334 mark that,modify
R2663 T8334 T8330 ccomp modify,confirm
R2664 T8335 T8336 compound MMU2,QTL
R2665 T8336 T8334 nsubj QTL,modify
R2666 T8337 T8338 det the,effects
R2667 T8338 T8334 dobj effects,modify
R2668 T8339 T8338 prep of,effects
R2669 T8340 T8341 det the,deletion
R2670 T8341 T8339 pobj deletion,of
R2671 T8342 T8341 compound hg,deletion
R2672 T8343 T8330 punct .,confirm
R2344 T7999 T8000 compound HG,genotype
R2612 T8287 T8288 mark although,reached
R2617 T8292 T8288 dobj significance,reached

craft-ca-core-ex-dev

Below, discontinuous spans are shown in the chain model. You can change it to the bag model.

Id Subject Object Predicate Lexical cue
T6925 16-19 SO_EXT:0000771 denotes QTL
T6926 133-136 SO_EXT:0000771 denotes QTL
T6927 167-175 SO_EXT:genotype_or_entity_with_genotype denotes genotype
T6928 248-255 SO_EXT:0000704 denotes genetic
T6929 273-274 SO_EXT:normal_or_wild_type_or_present denotes +
T6930 275-276 SO_EXT:normal_or_wild_type_or_present denotes +
T6931 347-355 SO_EXT:genotype_or_entity_with_genotype denotes genotype
T6932 404-407 SO_EXT:0000771 denotes QTL
T6933 434-441 SO_EXT:0001026 denotes genomic
T6934 495-499 SO_EXT:0000704 denotes gene
T6935 632-636 NCBITaxon:10088 denotes mice
T6936 839-842 SO_EXT:0000771 denotes QTL
T6937 867-869 SO_EXT:0000028 denotes bp
T6938 1048-1056 SO_EXT:genotype_or_entity_with_genotype denotes genotype
T6939 1122-1126 NCBITaxon:10088 denotes mice
T6940 1199-1203 NCBITaxon:10088 denotes mice
T6941 1239-1247 SO_EXT:genotype_or_entity_with_genotype denotes genotype
T6942 1397-1403 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes female
T6943 1428-1432 PATO_UBERON_EXT:male_or_bearer_of_maleness denotes male
T6944 1467-1470 CHEBI_UBERON_EXT:triglyceride_or_adipose_tissue denotes fat
T6945 1538-1546 SO_EXT:genotype_or_entity_with_genotype denotes genotype
T6946 1582-1590 SO_EXT:genotype_or_entity_with_genotype denotes genotype
T6947 1707-1715 SO_EXT:genotype_or_entity_with_genotype denotes genotype
T6948 2011-2014 SO_EXT:0000771 denotes QTL
T6949 2044-2052 SO_EXT:sequence_deletion_entity_or_process denotes deletion

craft-ca-core-dev

Below, discontinuous spans are shown in the chain model. You can change it to the bag model.

Id Subject Object Predicate Lexical cue
T6823 16-19 SO:0000771 denotes QTL
T6824 133-136 SO:0000771 denotes QTL
T6825 248-255 SO:0000704 denotes genetic
T6826 404-407 SO:0000771 denotes QTL
T6827 434-441 SO:0001026 denotes genomic
T6828 495-499 SO:0000704 denotes gene
T6829 632-636 NCBITaxon:10088 denotes mice
T6830 839-842 SO:0000771 denotes QTL
T6831 867-869 SO:0000028 denotes bp
T6832 1122-1126 NCBITaxon:10088 denotes mice
T6833 1199-1203 NCBITaxon:10088 denotes mice
T6834 2011-2014 SO:0000771 denotes QTL