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PMC:1482699 / 12292-12705 JSONTXT 3 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T7938 0-2 DT denotes An
T7940 3-12 JJ denotes important
T7939 13-20 NN denotes feature
T7942 21-23 IN denotes of
T7943 24-27 PRP$ denotes our
T7945 28-40 JJ denotes experimental
T7944 41-47 NN denotes design
T7941 48-51 VBD denotes was
T7946 52-55 DT denotes the
T7947 56-63 NN denotes ability
T7948 64-66 TO denotes to
T7949 67-71 VB denotes test
T7950 72-75 IN denotes for
T7951 76-88 NNS denotes interactions
T7952 89-96 IN denotes between
T7953 97-100 NN denotes QTL
T7954 101-103 IN denotes in
T7955 104-108 DT denotes each
T7957 109-113 NN denotes MMU2
T7958 114-119 NN denotes donor
T7956 120-126 NN denotes region
T7959 127-130 CC denotes and
T7960 131-139 VB denotes genotype
T7961 140-142 IN denotes at
T7962 143-146 DT denotes the
T7964 147-149 NN denotes HG
T7963 150-155 NN denotes locus
T7965 155-157 , denotes ,
T7966 157-162 IN denotes since
T7968 163-172 JJ denotes identical
T7970 173-178 NN denotes donor
T7969 179-186 NNS denotes regions
T7971 187-191 VBD denotes were
T7967 192-204 VBN denotes introgressed
T7972 205-207 IN denotes on
T7973 208-211 CD denotes two
T7975 212-219 JJ denotes genetic
T7974 220-231 NNS denotes backgrounds
T7976 231-233 , denotes ,
T7977 233-235 NN denotes B6
T7978 236-237 -LRB- denotes (
T7980 237-238 SYM denotes +
T7981 238-239 HYPH denotes /
T7979 239-240 SYM denotes +
T7982 240-241 -RRB- denotes )
T7983 242-245 CC denotes and
T7984 246-248 NN denotes HG
T7985 249-250 -LRB- denotes (
T7987 250-252 NN denotes hg
T7988 252-253 HYPH denotes /
T7986 253-255 NN denotes hg
T7989 255-256 -RRB- denotes )
T7990 256-257 . denotes .
T7991 257-413 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 258-269 JJ denotes Significant
T7993 270-282 NNS denotes interactions
T7995 283-290 IN denotes between
T7996 291-296 NN denotes donor
T7997 297-303 NN denotes region
T7998 304-307 CC denotes and
T7999 308-310 NN denotes HG
T8000 311-319 NN denotes genotype
T8001 320-324 VBD denotes were
T7994 325-331 VBN denotes viewed
T8002 332-334 IN denotes as
T8003 335-341 JJ denotes strong
T8004 342-350 NN denotes evidence
T8005 351-355 IN denotes that
T8007 356-358 NN denotes hg
T8009 359-367 NN denotes modifier
T8008 368-371 NN denotes QTL
T8006 372-378 VBP denotes reside
T8010 379-385 IN denotes within
T8011 386-390 DT denotes that
T8013 391-397 JJ denotes unique
T8014 398-405 JJ denotes genomic
T8012 406-412 NN denotes region
T8015 412-413 . denotes .
R2289 T7983 T7977 cc and,B6
R2294 T7984 T7977 conj HG,B6
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
R2344 T7999 T8000 compound HG,genotype
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
R2359 T8005 T8006 mark that,reside
R2363 T8006 T8004 acl reside,evidence
R2368 T8007 T8008 compound hg,QTL
R2371 T8008 T8006 nsubj QTL,reside
R2375 T8009 T8008 compound modifier,QTL
R2379 T8010 T8006 prep within,reside
R2383 T8011 T8012 det that,region
R2387 T8012 T8010 pobj region,within
R2391 T8013 T8012 amod unique,region
R2395 T8014 T8012 amod genomic,region
R2398 T8015 T7994 punct .,viewed