craft-sa-dev Home  

PMC:1860061 / 10399-11836 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T7097 0-2 IN denotes In
T7099 3-4 DT denotes a
T7101 5-13 JJ denotes previous
T7100 14-19 NN denotes study
T7102 19-21 , denotes ,
T7103 21-23 PRP denotes we
T7098 24-31 VBD denotes carried
T7104 32-35 RP denotes out
T7105 36-37 DT denotes a
T7107 38-44 NN denotes genome
T7106 45-51 NN denotes screen
T7108 52-54 TO denotes to
T7109 55-63 VB denotes identify
T7110 64-67 NN denotes QTL
T7111 68-79 VBG denotes controlling
T7112 80-83 NN denotes CIA
T7113 84-98 NN denotes susceptibility
T7114 99-101 IN denotes in
T7115 102-103 -LRB- denotes (
T7116 103-106 NN denotes DBA
T7118 106-107 HYPH denotes /
T7119 107-108 CD denotes 1
T7120 109-110 SYM denotes ×
T7122 111-114 NN denotes FVB
T7123 114-115 HYPH denotes /
T7121 115-116 NN denotes N
T7124 116-117 -RRB- denotes )
T7125 118-120 NN denotes F2
T7117 121-128 NN denotes progeny
T7126 128-129 . denotes .
T7127 129-278 sentence denotes For the phenotype of arthritis severity, only one QTL, Cia2, was identified, with a highly significant logarithm of the odds (LOD) score of 12 [10].
T7128 130-133 IN denotes For
T7130 134-137 DT denotes the
T7131 138-147 NN denotes phenotype
T7132 148-150 IN denotes of
T7133 151-160 NN denotes arthritis
T7134 161-169 NN denotes severity
T7135 169-171 , denotes ,
T7136 171-175 RB denotes only
T7138 176-179 CD denotes one
T7137 180-183 NN denotes QTL
T7139 183-185 , denotes ,
T7140 185-189 NN denotes Cia2
T7141 189-191 , denotes ,
T7142 191-194 VBD denotes was
T7129 195-205 VBN denotes identified
T7143 205-207 , denotes ,
T7144 207-211 IN denotes with
T7145 212-213 DT denotes a
T7147 214-220 RB denotes highly
T7148 221-232 JJ denotes significant
T7149 233-242 NN denotes logarithm
T7150 243-245 IN denotes of
T7151 246-249 DT denotes the
T7152 250-254 NNS denotes odds
T7153 255-256 -LRB- denotes (
T7154 256-259 NN denotes LOD
T7155 259-260 -RRB- denotes )
T7146 261-266 NN denotes score
T7156 267-269 IN denotes of
T7157 270-272 CD denotes 12
T7158 273-274 -LRB- denotes [
T7159 274-276 CD denotes 10
T7160 276-277 -RRB- denotes ]
T7161 277-278 . denotes .
T7162 278-499 sentence denotes However, Cia2 contributed to only 16% of the phenotype variations, indicating that there should be some small-effect QTL whose contributions to CIA were not big enough to reach the significant threshold value of linkage.
T7163 279-286 RB denotes However
T7165 286-288 , denotes ,
T7166 288-292 NN denotes Cia2
T7164 293-304 VBD denotes contributed
T7167 305-307 IN denotes to
T7168 308-312 RB denotes only
T7170 313-315 CD denotes 16
T7169 315-316 NN denotes %
T7171 317-319 IN denotes of
T7172 320-323 DT denotes the
T7174 324-333 NN denotes phenotype
T7173 334-344 NNS denotes variations
T7175 344-346 , denotes ,
T7176 346-356 VBG denotes indicating
T7177 357-361 IN denotes that
T7179 362-367 EX denotes there
T7180 368-374 MD denotes should
T7178 375-377 VB denotes be
T7181 378-382 DT denotes some
T7183 383-388 JJ denotes small
T7185 388-389 HYPH denotes -
T7184 389-395 NN denotes effect
T7182 396-399 NNS denotes QTL
T7186 400-405 WP$ denotes whose
T7187 406-419 NNS denotes contributions
T7189 420-422 IN denotes to
T7190 423-426 NN denotes CIA
T7188 427-431 VBD denotes were
T7191 432-435 RB denotes not
T7192 436-439 JJ denotes big
T7193 440-446 RB denotes enough
T7194 447-449 TO denotes to
T7195 450-455 VB denotes reach
T7196 456-459 DT denotes the
T7198 460-471 JJ denotes significant
T7199 472-481 NN denotes threshold
T7197 482-487 NN denotes value
T7200 488-490 IN denotes of
T7201 491-498 NN denotes linkage
T7202 498-499 . denotes .
T7203 499-621 sentence denotes To identify these potential small-effect QTL, we reanalyzed the data using a lower threshold value of linkage (P = 0.05).
T7204 500-502 TO denotes To
T7205 503-511 VB denotes identify
T7207 512-517 DT denotes these
T7209 518-527 JJ denotes potential
T7210 528-533 JJ denotes small
T7212 533-534 HYPH denotes -
T7211 534-540 NN denotes effect
T7208 541-544 NNS denotes QTL
T7213 544-546 , denotes ,
T7214 546-548 PRP denotes we
T7206 549-559 VBD denotes reanalyzed
T7215 560-563 DT denotes the
T7216 564-568 NNS denotes data
T7217 569-574 VBG denotes using
T7218 575-576 DT denotes a
T7220 577-582 JJR denotes lower
T7221 583-592 NN denotes threshold
T7219 593-598 NN denotes value
T7222 599-601 IN denotes of
T7223 602-609 NN denotes linkage
T7224 610-611 -LRB- denotes (
T7226 611-612 NN denotes P
T7227 613-614 SYM denotes =
T7225 615-619 CD denotes 0.05
T7228 619-620 -RRB- denotes )
T7229 620-621 . denotes .
T7230 621-855 sentence denotes We reasoned that since the main candidate gene of Cia2, complement component C5 (Hc), was proven to be essential for CIA development and because the FVB/N strain is C5 deficient [10,25], some small-effect QTL might be masked by Cia2.
T7231 622-624 PRP denotes We
T7232 625-633 VBD denotes reasoned
T7233 634-638 IN denotes that
T7235 639-644 IN denotes since
T7237 645-648 DT denotes the
T7239 649-653 JJ denotes main
T7240 654-663 NN denotes candidate
T7238 664-668 NN denotes gene
T7241 669-671 IN denotes of
T7242 672-676 NN denotes Cia2
T7243 676-678 , denotes ,
T7244 678-688 NN denotes complement
T7246 689-698 NN denotes component
T7245 699-701 NN denotes C5
T7247 702-703 -LRB- denotes (
T7248 703-705 NN denotes Hc
T7249 705-706 -RRB- denotes )
T7250 706-708 , denotes ,
T7251 708-711 VBD denotes was
T7236 712-718 VBN denotes proven
T7252 719-721 TO denotes to
T7253 722-724 VB denotes be
T7254 725-734 JJ denotes essential
T7255 735-738 IN denotes for
T7256 739-742 NN denotes CIA
T7257 743-754 NN denotes development
T7258 755-758 CC denotes and
T7259 759-766 IN denotes because
T7261 767-770 DT denotes the
T7263 771-774 NN denotes FVB
T7265 774-775 HYPH denotes /
T7264 775-776 NN denotes N
T7262 777-783 NN denotes strain
T7260 784-786 VBZ denotes is
T7266 787-789 NN denotes C5
T7267 790-799 JJ denotes deficient
T7268 800-801 -LRB- denotes [
T7270 801-803 CD denotes 10
T7271 803-804 , denotes ,
T7269 804-806 CD denotes 25
T7272 806-807 -RRB- denotes ]
T7273 807-809 , denotes ,
T7274 809-813 DT denotes some
T7276 814-819 JJ denotes small
T7278 819-820 HYPH denotes -
T7277 820-826 NN denotes effect
T7275 827-830 NNS denotes QTL
T7279 831-836 MD denotes might
T7280 837-839 VB denotes be
T7234 840-846 VBN denotes masked
T7281 847-849 IN denotes by
T7282 850-854 NN denotes Cia2
T7283 854-855 . denotes .
T7284 855-1047 sentence denotes To exclude the masking effect of C5, we performed linkage analysis with 3 datasets, the first containing all 290 F2 progeny, the second 77 C5+/+ F2 progeny and the third 133 C5+/- F2 progeny.
T7285 856-858 TO denotes To
T7286 859-866 VB denotes exclude
T7288 867-870 DT denotes the
T7290 871-878 NN denotes masking
T7289 879-885 NN denotes effect
T7291 886-888 IN denotes of
T7292 889-891 NN denotes C5
T7293 891-893 , denotes ,
T7294 893-895 PRP denotes we
T7287 896-905 VBD denotes performed
T7295 906-913 NN denotes linkage
T7296 914-922 NN denotes analysis
T7297 923-927 IN denotes with
T7298 928-929 CD denotes 3
T7299 930-938 NNS denotes datasets
T7300 938-940 , denotes ,
T7301 940-943 DT denotes the
T7302 944-949 JJ denotes first
T7303 950-960 VBG denotes containing
T7304 961-964 DT denotes all
T7306 965-968 CD denotes 290
T7307 969-971 NN denotes F2
T7305 972-979 NN denotes progeny
T7308 979-981 , denotes ,
T7309 981-984 DT denotes the
T7310 985-991 JJ denotes second
T7312 992-994 CD denotes 77
T7313 995-998 NN denotes C5+
T7314 998-999 HYPH denotes /
T7315 999-1000 SYM denotes +
T7316 1001-1003 NN denotes F2
T7311 1004-1011 NN denotes progeny
T7317 1012-1015 CC denotes and
T7318 1016-1019 DT denotes the
T7319 1020-1025 JJ denotes third
T7321 1026-1029 CD denotes 133
T7322 1030-1033 NN denotes C5+
T7323 1033-1034 HYPH denotes /
T7324 1034-1035 SYM denotes -
T7325 1036-1038 NN denotes F2
T7320 1039-1046 NN denotes progeny
T7326 1046-1047 . denotes .
T7327 1047-1185 sentence denotes Eight genomic regions were linked to the phenotype of CIA severity (loci 1 to 8, Table 2), with P values varying between 0.043 and 0.003.
T7328 1048-1053 CD denotes Eight
T7330 1054-1061 JJ denotes genomic
T7329 1062-1069 NNS denotes regions
T7332 1070-1074 VBD denotes were
T7331 1075-1081 VBN denotes linked
T7333 1082-1084 IN denotes to
T7334 1085-1088 DT denotes the
T7335 1089-1098 NN denotes phenotype
T7336 1099-1101 IN denotes of
T7337 1102-1105 NN denotes CIA
T7338 1106-1114 NN denotes severity
T7339 1115-1116 -LRB- denotes (
T7341 1116-1120 NNS denotes loci
T7342 1121-1122 CD denotes 1
T7343 1123-1125 IN denotes to
T7344 1126-1127 CD denotes 8
T7345 1127-1129 , denotes ,
T7340 1129-1134 NN denotes Table
T7346 1135-1136 CD denotes 2
T7347 1136-1137 -RRB- denotes )
T7348 1137-1139 , denotes ,
T7349 1139-1143 IN denotes with
T7351 1144-1145 NN denotes P
T7352 1146-1152 NNS denotes values
T7350 1153-1160 VBG denotes varying
T7353 1161-1168 IN denotes between
T7354 1169-1174 CD denotes 0.043
T7355 1175-1178 CC denotes and
T7356 1179-1184 CD denotes 0.003
T7357 1184-1185 . denotes .
T7358 1185-1271 sentence denotes These eight small-effect QTL were located on chromosomes 5, 6, 7, 10, 11, 16, and 17.
T7359 1186-1191 DT denotes These
T7361 1192-1197 CD denotes eight
T7362 1198-1203 JJ denotes small
T7364 1203-1204 HYPH denotes -
T7363 1204-1210 NN denotes effect
T7360 1211-1214 NNS denotes QTL
T7366 1215-1219 VBD denotes were
T7365 1220-1227 VBN denotes located
T7367 1228-1230 IN denotes on
T7368 1231-1242 NNS denotes chromosomes
T7369 1243-1244 CD denotes 5
T7370 1244-1246 , denotes ,
T7371 1246-1247 CD denotes 6
T7372 1247-1249 , denotes ,
T7373 1249-1250 CD denotes 7
T7374 1250-1252 , denotes ,
T7375 1252-1254 CD denotes 10
T7376 1254-1256 , denotes ,
T7377 1256-1258 CD denotes 11
T7378 1258-1260 , denotes ,
T7379 1260-1262 CD denotes 16
T7380 1262-1264 , denotes ,
T7381 1264-1267 CC denotes and
T7382 1268-1270 CD denotes 17
T7383 1270-1271 . denotes .
T7384 1271-1323 sentence denotes Five loci were identified in at least two datasets.
T7385 1272-1276 CD denotes Five
T7386 1277-1281 NNS denotes loci
T7388 1282-1286 VBD denotes were
T7387 1287-1297 VBN denotes identified
T7389 1298-1300 IN denotes in
T7390 1301-1303 RB denotes at
T7392 1304-1309 RBS denotes least
T7391 1310-1313 CD denotes two
T7393 1314-1322 NNS denotes datasets
T7394 1322-1323 . denotes .
T7395 1323-1437 sentence denotes Of the eight loci, five had DBA/1 as the susceptibility allele, and three had FVB/N as the susceptibility allele.
T7396 1324-1326 IN denotes Of
T7398 1327-1330 DT denotes the
T7400 1331-1336 CD denotes eight
T7399 1337-1341 NNS denotes loci
T7401 1341-1343 , denotes ,
T7402 1343-1347 CD denotes five
T7397 1348-1351 VBD denotes had
T7403 1352-1355 NN denotes DBA
T7404 1355-1356 HYPH denotes /
T7405 1356-1357 CD denotes 1
T7406 1358-1360 IN denotes as
T7407 1361-1364 DT denotes the
T7409 1365-1379 NN denotes susceptibility
T7408 1380-1386 NN denotes allele
T7410 1386-1388 , denotes ,
T7411 1388-1391 CC denotes and
T7412 1392-1397 CD denotes three
T7413 1398-1401 VBD denotes had
T7414 1402-1405 NN denotes FVB
T7416 1405-1406 HYPH denotes /
T7415 1406-1407 NN denotes N
T7417 1408-1410 IN denotes as
T7418 1411-1414 DT denotes the
T7420 1415-1429 NN denotes susceptibility
T7419 1430-1436 NN denotes allele
T7421 1436-1437 . denotes .
R1841 T7097 T7098 prep In,carried
R1842 T7099 T7100 det a,study
R1843 T7100 T7097 pobj study,In
R1844 T7101 T7100 amod previous,study
R1845 T7102 T7098 punct ", ",carried
R1846 T7103 T7098 nsubj we,carried
R1847 T7104 T7098 prt out,carried
R1848 T7105 T7106 det a,screen
R1849 T7106 T7098 dobj screen,carried
R1850 T7107 T7106 compound genome,screen
R1851 T7108 T7109 aux to,identify
R1852 T7109 T7098 advcl identify,carried
R1853 T7110 T7109 dobj QTL,identify
R1854 T7111 T7110 acl controlling,QTL
R1855 T7112 T7113 compound CIA,susceptibility
R1856 T7113 T7111 dobj susceptibility,controlling
R1857 T7114 T7111 prep in,controlling
R1858 T7115 T7116 punct (,DBA
R1859 T7116 T7117 nmod DBA,progeny
R1860 T7117 T7114 pobj progeny,in
R1861 T7118 T7116 punct /,DBA
R1862 T7119 T7116 nummod 1,DBA
R1863 T7120 T7121 punct ×,N
R1864 T7121 T7116 prep N,DBA
R1865 T7122 T7121 compound FVB,N
R1866 T7123 T7121 punct /,N
R1867 T7124 T7116 punct ),DBA
R1868 T7125 T7117 compound F2,progeny
R1869 T7126 T7098 punct .,carried
R1870 T7128 T7129 prep For,identified
R1871 T7130 T7131 det the,phenotype
R1872 T7131 T7128 pobj phenotype,For
R1873 T7132 T7131 prep of,phenotype
R1874 T7133 T7134 compound arthritis,severity
R1875 T7134 T7132 pobj severity,of
R1876 T7135 T7129 punct ", ",identified
R1877 T7136 T7137 advmod only,QTL
R1878 T7137 T7129 nsubjpass QTL,identified
R1879 T7138 T7137 nummod one,QTL
R1880 T7139 T7137 punct ", ",QTL
R1881 T7140 T7137 appos Cia2,QTL
R1882 T7141 T7129 punct ", ",identified
R1883 T7142 T7129 auxpass was,identified
R1884 T7143 T7129 punct ", ",identified
R1885 T7144 T7129 prep with,identified
R1886 T7145 T7146 det a,score
R1887 T7146 T7144 pobj score,with
R1888 T7147 T7148 advmod highly,significant
R1889 T7148 T7146 amod significant,score
R1890 T7149 T7146 nmod logarithm,score
R1891 T7150 T7149 prep of,logarithm
R1892 T7151 T7152 det the,odds
R1893 T7152 T7150 pobj odds,of
R1894 T7153 T7149 punct (,logarithm
R1895 T7154 T7149 appos LOD,logarithm
R1896 T7155 T7146 punct ),score
R1897 T7156 T7146 prep of,score
R1898 T7157 T7156 pobj 12,of
R1899 T7158 T7159 punct [,10
R1900 T7159 T7129 parataxis 10,identified
R1901 T7160 T7159 punct ],10
R1902 T7161 T7129 punct .,identified
R1903 T7163 T7164 advmod However,contributed
R1904 T7165 T7164 punct ", ",contributed
R1905 T7166 T7164 nsubj Cia2,contributed
R1906 T7167 T7164 prep to,contributed
R1907 T7168 T7169 advmod only,%
R1908 T7169 T7167 pobj %,to
R1909 T7170 T7169 nummod 16,%
R1910 T7171 T7169 prep of,%
R1911 T7172 T7173 det the,variations
R1912 T7173 T7171 pobj variations,of
R1913 T7174 T7173 compound phenotype,variations
R1914 T7175 T7164 punct ", ",contributed
R1915 T7176 T7164 advcl indicating,contributed
R1916 T7177 T7178 mark that,be
R1917 T7178 T7176 ccomp be,indicating
R1918 T7179 T7178 expl there,be
R1919 T7180 T7178 aux should,be
R1920 T7181 T7182 det some,QTL
R1921 T7182 T7178 attr QTL,be
R1922 T7183 T7184 amod small,effect
R1923 T7184 T7182 compound effect,QTL
R1924 T7185 T7184 punct -,effect
R1925 T7186 T7187 poss whose,contributions
R1926 T7187 T7188 dep contributions,were
R1927 T7188 T7182 relcl were,QTL
R1928 T7189 T7187 prep to,contributions
R1929 T7190 T7189 pobj CIA,to
R1930 T7191 T7188 neg not,were
R1931 T7192 T7188 acomp big,were
R1932 T7193 T7192 advmod enough,big
R1933 T7194 T7195 aux to,reach
R1934 T7195 T7192 xcomp reach,big
R1935 T7196 T7197 det the,value
R1936 T7197 T7195 dobj value,reach
R1937 T7198 T7199 amod significant,threshold
R1938 T7199 T7197 compound threshold,value
R1939 T7200 T7197 prep of,value
R1940 T7201 T7200 pobj linkage,of
R1941 T7202 T7164 punct .,contributed
R1942 T7204 T7205 aux To,identify
R1943 T7205 T7206 advcl identify,reanalyzed
R1944 T7207 T7208 det these,QTL
R1945 T7208 T7205 dobj QTL,identify
R1946 T7209 T7208 amod potential,QTL
R1947 T7210 T7211 amod small,effect
R1948 T7211 T7208 compound effect,QTL
R1949 T7212 T7211 punct -,effect
R1950 T7213 T7206 punct ", ",reanalyzed
R1951 T7214 T7206 nsubj we,reanalyzed
R1952 T7215 T7216 det the,data
R1953 T7216 T7206 dobj data,reanalyzed
R1954 T7217 T7206 advcl using,reanalyzed
R1955 T7218 T7219 det a,value
R1956 T7219 T7217 dobj value,using
R1957 T7220 T7221 amod lower,threshold
R1958 T7221 T7219 compound threshold,value
R1959 T7222 T7219 prep of,value
R1960 T7223 T7222 pobj linkage,of
R1961 T7224 T7225 punct (,0.05
R1962 T7225 T7219 parataxis 0.05,value
R1963 T7226 T7225 nsubj P,0.05
R1964 T7227 T7225 punct =,0.05
R1965 T7228 T7225 punct ),0.05
R1966 T7229 T7206 punct .,reanalyzed
R1967 T7231 T7232 nsubj We,reasoned
R1968 T7233 T7234 mark that,masked
R1969 T7234 T7232 ccomp masked,reasoned
R1970 T7235 T7236 mark since,proven
R1971 T7236 T7234 advcl proven,masked
R1972 T7237 T7238 det the,gene
R1973 T7238 T7236 nsubjpass gene,proven
R1974 T7239 T7238 amod main,gene
R1975 T7240 T7238 compound candidate,gene
R1976 T7241 T7238 prep of,gene
R1977 T7242 T7241 pobj Cia2,of
R1978 T7243 T7238 punct ", ",gene
R1979 T7244 T7245 compound complement,C5
R1980 T7245 T7238 appos C5,gene
R1981 T7246 T7245 compound component,C5
R1982 T7247 T7248 punct (,Hc
R1983 T7248 T7245 parataxis Hc,C5
R1984 T7249 T7248 punct ),Hc
R1985 T7250 T7236 punct ", ",proven
R1986 T7251 T7236 auxpass was,proven
R1987 T7252 T7253 aux to,be
R1988 T7253 T7236 xcomp be,proven
R1989 T7254 T7253 acomp essential,be
R1990 T7255 T7254 prep for,essential
R1991 T7256 T7257 compound CIA,development
R1992 T7257 T7255 pobj development,for
R1993 T7258 T7236 cc and,proven
R1994 T7259 T7260 mark because,is
R1995 T7260 T7236 conj is,proven
R1996 T7261 T7262 det the,strain
R1997 T7262 T7260 nsubj strain,is
R1998 T7263 T7264 compound FVB,N
R1999 T7264 T7262 compound N,strain
R2000 T7265 T7264 punct /,N
R2001 T7266 T7267 npadvmod C5,deficient
R2002 T7267 T7260 acomp deficient,is
R2003 T7268 T7269 punct [,25
R2004 T7269 T7260 parataxis 25,is
R2005 T7270 T7269 nummod 10,25
R2006 T7271 T7269 punct ",",25
R2007 T7272 T7269 punct ],25
R2008 T7273 T7234 punct ", ",masked
R2009 T7274 T7275 det some,QTL
R2010 T7275 T7234 nsubjpass QTL,masked
R2011 T7276 T7277 amod small,effect
R2012 T7277 T7275 compound effect,QTL
R2013 T7278 T7277 punct -,effect
R2014 T7279 T7234 aux might,masked
R2015 T7280 T7234 auxpass be,masked
R2016 T7281 T7234 agent by,masked
R2017 T7282 T7281 pobj Cia2,by
R2018 T7283 T7232 punct .,reasoned
R2019 T7285 T7286 aux To,exclude
R2020 T7286 T7287 advcl exclude,performed
R2021 T7288 T7289 det the,effect
R2022 T7289 T7286 dobj effect,exclude
R2023 T7290 T7289 compound masking,effect
R2024 T7291 T7289 prep of,effect
R2025 T7292 T7291 pobj C5,of
R2026 T7293 T7287 punct ", ",performed
R2027 T7294 T7287 nsubj we,performed
R2028 T7295 T7296 compound linkage,analysis
R2029 T7296 T7287 dobj analysis,performed
R2030 T7297 T7287 prep with,performed
R2031 T7298 T7299 nummod 3,datasets
R2032 T7299 T7297 pobj datasets,with
R2033 T7300 T7287 punct ", ",performed
R2034 T7301 T7302 det the,first
R2035 T7302 T7303 nsubj first,containing
R2036 T7303 T7287 advcl containing,performed
R2037 T7304 T7305 det all,progeny
R2038 T7305 T7303 dobj progeny,containing
R2039 T7306 T7305 nummod 290,progeny
R2040 T7307 T7305 compound F2,progeny
R2041 T7308 T7303 punct ", ",containing
R2042 T7309 T7310 det the,second
R2043 T7310 T7311 nsubj second,progeny
R2044 T7311 T7303 conj progeny,containing
R2045 T7312 T7311 nummod 77,progeny
R2046 T7313 T7311 nmod C5+,progeny
R2047 T7314 T7313 punct /,C5+
R2048 T7315 T7313 punct +,C5+
R2049 T7316 T7311 compound F2,progeny
R2050 T7317 T7311 cc and,progeny
R2051 T7318 T7319 det the,third
R2052 T7319 T7320 nsubj third,progeny
R2053 T7320 T7311 conj progeny,progeny
R2054 T7321 T7320 nummod 133,progeny
R2055 T7322 T7320 nmod C5+,progeny
R2056 T7323 T7322 punct /,C5+
R2057 T7324 T7322 punct -,C5+
R2058 T7325 T7320 compound F2,progeny
R2059 T7326 T7287 punct .,performed
R2060 T7328 T7329 nummod Eight,regions
R2061 T7329 T7331 nsubjpass regions,linked
R2062 T7330 T7329 amod genomic,regions
R2063 T7332 T7331 auxpass were,linked
R2064 T7333 T7331 prep to,linked
R2065 T7334 T7335 det the,phenotype
R2066 T7335 T7333 pobj phenotype,to
R2067 T7336 T7335 prep of,phenotype
R2068 T7337 T7338 compound CIA,severity
R2069 T7338 T7336 pobj severity,of
R2070 T7339 T7340 punct (,Table
R2071 T7340 T7331 parataxis Table,linked
R2072 T7341 T7342 nmod loci,1
R2073 T7342 T7340 dep 1,Table
R2074 T7343 T7342 prep to,1
R2075 T7344 T7343 pobj 8,to
R2076 T7345 T7340 punct ", ",Table
R2077 T7346 T7340 nummod 2,Table
R2078 T7347 T7340 punct ),Table
R2079 T7348 T7331 punct ", ",linked
R2080 T7349 T7350 mark with,varying
R2081 T7350 T7331 advcl varying,linked
R2082 T7351 T7352 compound P,values
R2083 T7352 T7350 nsubj values,varying
R2084 T7353 T7350 prep between,varying
R2085 T7354 T7353 pobj 0.043,between
R2086 T7355 T7354 cc and,0.043
R2087 T7356 T7354 conj 0.003,0.043
R2088 T7357 T7331 punct .,linked
R2089 T7359 T7360 det These,QTL
R2090 T7360 T7365 nsubjpass QTL,located
R2091 T7361 T7360 nummod eight,QTL
R2092 T7362 T7363 amod small,effect
R2093 T7363 T7360 compound effect,QTL
R2094 T7364 T7363 punct -,effect
R2095 T7366 T7365 auxpass were,located
R2096 T7367 T7365 prep on,located
R2097 T7368 T7369 nmod chromosomes,5
R2098 T7369 T7367 pobj 5,on
R2099 T7370 T7369 punct ", ",5
R2100 T7371 T7369 conj 6,5
R2101 T7372 T7371 punct ", ",6
R2102 T7373 T7371 conj 7,6
R2103 T7374 T7373 punct ", ",7
R2104 T7375 T7373 conj 10,7
R2105 T7376 T7375 punct ", ",10
R2106 T7377 T7375 conj 11,10
R2107 T7378 T7377 punct ", ",11
R2108 T7379 T7377 conj 16,11
R2109 T7380 T7379 punct ", ",16
R2110 T7381 T7379 cc and,16
R2111 T7382 T7379 conj 17,16
R2112 T7383 T7365 punct .,located
R2113 T7385 T7386 nummod Five,loci
R2114 T7386 T7387 nsubjpass loci,identified
R2115 T7388 T7387 auxpass were,identified
R2116 T7389 T7387 prep in,identified
R2117 T7390 T7391 advmod at,two
R2118 T7391 T7393 nummod two,datasets
R2119 T7392 T7391 advmod least,two
R2120 T7393 T7389 pobj datasets,in
R2121 T7394 T7387 punct .,identified
R2122 T7396 T7397 prep Of,had
R2123 T7398 T7399 det the,loci
R2124 T7399 T7396 pobj loci,Of
R2125 T7400 T7399 nummod eight,loci
R2126 T7401 T7397 punct ", ",had
R2127 T7402 T7397 nsubj five,had
R2128 T7403 T7397 dobj DBA,had
R2129 T7404 T7403 punct /,DBA
R2130 T7405 T7403 nummod 1,DBA
R2131 T7406 T7397 prep as,had
R2132 T7407 T7408 det the,allele
R2133 T7408 T7406 pobj allele,as
R2134 T7409 T7408 compound susceptibility,allele
R2135 T7410 T7397 punct ", ",had
R2136 T7411 T7397 cc and,had
R2137 T7412 T7413 nsubj three,had
R2138 T7413 T7397 conj had,had
R2139 T7414 T7415 compound FVB,N
R2140 T7415 T7413 dobj N,had
R2141 T7416 T7415 punct /,N
R2142 T7417 T7413 prep as,had
R2143 T7418 T7419 det the,allele
R2144 T7419 T7417 pobj allele,as
R2145 T7420 T7419 compound susceptibility,allele
R2146 T7421 T7397 punct .,had