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PMC:1482699 / 29313-30873 JSONTXT

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Id Subject Object Predicate Lexical cue
T18970 0-3 DT denotes The
T18971 9-15 NN denotes strain
T18972 4-8 NN denotes HG11
T18973 16-18 VBZ denotes is
T18974 19-21 IN denotes of
T18975 22-32 JJ denotes particular
T18976 33-41 NN denotes interest
T18977 42-45 IN denotes for
T18978 46-47 DT denotes a
T18979 48-54 NN denotes number
T18980 55-57 IN denotes of
T18981 58-65 NNS denotes reasons
T18982 65-66 . denotes .
T18983 66-168 sentence denotes First, HG11 congenic mice demonstrated significant strain by sex interactions for a number of traits.
T18984 67-72 RB denotes First
T18985 93-105 VBD denotes demonstrated
T18986 72-74 , denotes ,
T18987 74-78 NN denotes HG11
T18988 79-87 JJ denotes congenic
T18989 88-92 NNS denotes mice
T18990 106-117 JJ denotes significant
T18991 132-144 NNS denotes interactions
T18992 118-124 NN denotes strain
T18993 125-127 IN denotes by
T18994 128-131 NN denotes sex
T18995 145-148 IN denotes for
T18996 149-150 DT denotes a
T18997 151-157 NN denotes number
T18998 158-160 IN denotes of
T18999 161-167 NNS denotes traits
T19000 167-168 . denotes .
T19001 168-261 sentence denotes Males were generally larger, faster growing and longer and the converse was seen in females.
T19002 169-174 NNS denotes Males
T19003 175-179 VBD denotes were
T19004 180-189 RB denotes generally
T19005 190-196 JJR denotes larger
T19006 196-198 , denotes ,
T19007 198-204 JJR denotes faster
T19008 205-212 VBG denotes growing
T19009 213-216 CC denotes and
T19010 217-223 JJR denotes longer
T19011 224-227 CC denotes and
T19012 228-231 DT denotes the
T19013 232-240 NN denotes converse
T19014 245-249 VBN denotes seen
T19015 241-244 VBD denotes was
T19016 250-252 IN denotes in
T19017 253-260 NNS denotes females
T19018 260-261 . denotes .
T19019 261-423 sentence denotes The confounding effects of sex are likely the reason for the discrepancies between the congenic and genome scan results, where both sexes were analyzed together.
T19020 262-265 DT denotes The
T19021 278-285 NNS denotes effects
T19022 266-277 VBG denotes confounding
T19023 293-296 VBP denotes are
T19024 286-288 IN denotes of
T19025 289-292 NN denotes sex
T19026 297-303 RB denotes likely
T19027 304-307 DT denotes the
T19028 308-314 NN denotes reason
T19029 315-318 IN denotes for
T19030 319-322 DT denotes the
T19031 323-336 NNS denotes discrepancies
T19032 337-344 IN denotes between
T19033 345-348 DT denotes the
T19034 374-381 NNS denotes results
T19035 349-357 JJ denotes congenic
T19036 362-368 NN denotes genome
T19037 358-361 CC denotes and
T19038 369-373 NN denotes scan
T19039 381-383 , denotes ,
T19040 383-388 WRB denotes where
T19041 405-413 VBN denotes analyzed
T19042 389-393 DT denotes both
T19043 394-399 NNS denotes sexes
T19044 400-404 VBD denotes were
T19045 414-422 RB denotes together
T19046 422-423 . denotes .
T19047 423-594 sentence denotes Secondly, Carp2 was found to interact with hg and MMU11 is saturated with genes involved in the central Gh intracellular signaling pathway, such as Gh, Stat5b and Stat5a.
T19048 424-432 RB denotes Secondly
T19049 444-449 VBN denotes found
T19050 432-434 , denotes ,
T19051 434-439 NN denotes Carp2
T19052 440-443 VBD denotes was
T19053 450-452 TO denotes to
T19054 453-461 VB denotes interact
T19055 462-466 IN denotes with
T19056 467-469 NN denotes hg
T19057 470-473 CC denotes and
T19058 474-479 NN denotes MMU11
T19059 483-492 VBN denotes saturated
T19060 480-482 VBZ denotes is
T19061 493-497 IN denotes with
T19062 498-503 NNS denotes genes
T19063 504-512 VBN denotes involved
T19064 513-515 IN denotes in
T19065 516-519 DT denotes the
T19066 555-562 NN denotes pathway
T19067 520-527 JJ denotes central
T19068 528-530 NN denotes Gh
T19069 531-544 JJ denotes intracellular
T19070 545-554 NN denotes signaling
T19071 562-564 , denotes ,
T19072 564-568 JJ denotes such
T19073 569-571 IN denotes as
T19074 572-574 NN denotes Gh
T19075 574-576 , denotes ,
T19076 576-582 NN denotes Stat5b
T19077 583-586 CC denotes and
T19078 587-593 NN denotes Stat5a
T19079 593-594 . denotes .
T19080 594-720 sentence denotes Thirdly, MMU11 growth QTL overlapping HG11 have been identified in a number of crosses using different mouse strains [37-41].
T19081 595-602 RB denotes Thirdly
T19082 648-658 VBN denotes identified
T19083 602-604 , denotes ,
T19084 604-609 NN denotes MMU11
T19085 617-620 NN denotes QTL
T19086 610-616 NN denotes growth
T19087 621-632 VBG denotes overlapping
T19088 633-637 NN denotes HG11
T19089 638-642 VBP denotes have
T19090 643-647 VBN denotes been
T19091 659-661 IN denotes in
T19092 662-663 DT denotes a
T19093 664-670 NN denotes number
T19094 671-673 IN denotes of
T19095 674-681 NNS denotes crosses
T19096 682-687 VBG denotes using
T19097 688-697 JJ denotes different
T19098 704-711 NNS denotes strains
T19099 698-703 NN denotes mouse
T19100 712-713 -LRB- denotes [
T19101 713-715 CD denotes 37
T19102 715-716 SYM denotes -
T19103 716-718 CD denotes 41
T19104 718-719 -RRB- denotes ]
T19105 719-720 . denotes .
T19106 720-957 sentence denotes Given the well documented sexually dimorphic nature of Gh secretion and Gh induced gene expression [42,43], it is probable that the underlying mutation in the HG11 congenic may reside in a gene enhancing Gh induced sex-specific effects.
T19107 721-726 VBN denotes Given
T19108 832-834 VBZ denotes is
T19109 727-730 DT denotes the
T19110 766-772 NN denotes nature
T19111 731-735 RB denotes well
T19112 736-746 VBN denotes documented
T19113 747-755 RB denotes sexually
T19114 756-765 JJ denotes dimorphic
T19115 773-775 IN denotes of
T19116 776-778 NN denotes Gh
T19117 779-788 NN denotes secretion
T19118 789-792 CC denotes and
T19119 793-795 NN denotes Gh
T19120 796-803 VBN denotes induced
T19121 809-819 NN denotes expression
T19122 804-808 NN denotes gene
T19123 820-821 -LRB- denotes [
T19124 824-826 CD denotes 43
T19125 821-823 CD denotes 42
T19126 823-824 , denotes ,
T19127 826-827 -RRB- denotes ]
T19128 827-829 , denotes ,
T19129 829-831 PRP denotes it
T19130 835-843 JJ denotes probable
T19131 844-848 IN denotes that
T19132 898-904 VB denotes reside
T19133 849-852 DT denotes the
T19134 864-872 NN denotes mutation
T19135 853-863 VBG denotes underlying
T19136 873-875 IN denotes in
T19137 876-879 DT denotes the
T19138 880-884 NN denotes HG11
T19139 885-893 JJ denotes congenic
T19140 894-897 MD denotes may
T19141 905-907 IN denotes in
T19142 908-909 DT denotes a
T19143 910-914 NN denotes gene
T19144 915-924 VBG denotes enhancing
T19145 925-927 NN denotes Gh
T19146 928-935 VBN denotes induced
T19147 949-956 NNS denotes effects
T19148 936-939 NN denotes sex
T19149 940-948 JJ denotes specific
T19150 939-940 HYPH denotes -
T19151 956-957 . denotes .
T19152 957-1024 sentence denotes The structural Gh gene itself and Stat5b are excellent candidates.
T19153 958-961 DT denotes The
T19154 976-980 NN denotes gene
T19155 962-972 JJ denotes structural
T19156 973-975 NN denotes Gh
T19157 999-1002 VBP denotes are
T19158 981-987 PRP denotes itself
T19159 988-991 CC denotes and
T19160 992-998 NN denotes Stat5b
T19161 1003-1012 JJ denotes excellent
T19162 1013-1023 NNS denotes candidates
T19163 1023-1024 . denotes .
T19164 1024-1180 sentence denotes The potential role of Gh would include polymorphism that alters protein function in the absence of Socs2 or that causes transcriptional deregulation of Gh.
T19165 1025-1028 DT denotes The
T19166 1039-1043 NN denotes role
T19167 1029-1038 JJ denotes potential
T19168 1056-1063 VB denotes include
T19169 1044-1046 IN denotes of
T19170 1047-1049 NN denotes Gh
T19171 1050-1055 MD denotes would
T19172 1064-1076 NN denotes polymorphism
T19173 1077-1081 WDT denotes that
T19174 1082-1088 VBZ denotes alters
T19175 1089-1096 NN denotes protein
T19176 1097-1105 NN denotes function
T19177 1106-1108 IN denotes in
T19178 1109-1112 DT denotes the
T19179 1113-1120 NN denotes absence
T19180 1121-1123 IN denotes of
T19181 1124-1129 NN denotes Socs2
T19182 1130-1132 CC denotes or
T19183 1133-1137 DT denotes that
T19184 1138-1144 VBZ denotes causes
T19185 1145-1160 JJ denotes transcriptional
T19186 1161-1173 NN denotes deregulation
T19187 1174-1176 IN denotes of
T19188 1177-1179 NN denotes Gh
T19189 1179-1180 . denotes .
T19190 1180-1391 sentence denotes Additionally, functional variation in Stat5b may explain the sex-specific phenotypes in HG11 mice since it is the primary transcription factor responsible for Gh induced sex-specific liver gene expression [44].
T19191 1181-1193 RB denotes Additionally
T19192 1230-1237 VB denotes explain
T19193 1193-1195 , denotes ,
T19194 1195-1205 JJ denotes functional
T19195 1206-1215 NN denotes variation
T19196 1216-1218 IN denotes in
T19197 1219-1225 NN denotes Stat5b
T19198 1226-1229 MD denotes may
T19199 1238-1241 DT denotes the
T19200 1255-1265 NNS denotes phenotypes
T19201 1242-1245 NN denotes sex
T19202 1246-1254 JJ denotes specific
T19203 1245-1246 HYPH denotes -
T19204 1266-1268 IN denotes in
T19205 1269-1273 NN denotes HG11
T19206 1274-1278 NNS denotes mice
T19207 1279-1284 IN denotes since
T19208 1288-1290 VBZ denotes is
T19209 1285-1287 PRP denotes it
T19210 1291-1294 DT denotes the
T19211 1317-1323 NN denotes factor
T19212 1295-1302 JJ denotes primary
T19213 1303-1316 NN denotes transcription
T19214 1324-1335 JJ denotes responsible
T19215 1336-1339 IN denotes for
T19216 1340-1342 NN denotes Gh
T19217 1343-1350 VBN denotes induced
T19218 1375-1385 NN denotes expression
T19219 1351-1354 NN denotes sex
T19220 1355-1363 JJ denotes specific
T19221 1354-1355 HYPH denotes -
T19222 1364-1369 NN denotes liver
T19223 1370-1374 NN denotes gene
T19224 1386-1387 -LRB- denotes [
T19225 1387-1389 CD denotes 44
T19226 1389-1390 -RRB- denotes ]
T19227 1390-1391 . denotes .
T19228 1391-1560 sentence denotes Future studies aimed at identifying the HG11 QTG, will certainly include a thorough characterization of Gh and Stat5b sequence and expression patterns in congenic mice.
T19229 1392-1398 JJ denotes Future
T19230 1399-1406 NNS denotes studies
T19231 1457-1464 VB denotes include
T19232 1407-1412 VBN denotes aimed
T19233 1413-1415 IN denotes at
T19234 1416-1427 VBG denotes identifying
T19235 1428-1431 DT denotes the
T19236 1437-1440 NN denotes QTG
T19237 1432-1436 NN denotes HG11
T19238 1440-1442 , denotes ,
T19239 1442-1446 MD denotes will
T19240 1447-1456 RB denotes certainly
T19241 1465-1466 DT denotes a
T19242 1476-1492 NN denotes characterization
T19243 1467-1475 JJ denotes thorough
T19244 1493-1495 IN denotes of
T19245 1496-1498 NN denotes Gh
T19246 1534-1542 NNS denotes patterns
T19247 1499-1502 CC denotes and
T19248 1503-1509 NN denotes Stat5b
T19249 1510-1518 NN denotes sequence
T19250 1519-1522 CC denotes and
T19251 1523-1533 NN denotes expression
T19252 1543-1545 IN denotes in
T19253 1546-1554 JJ denotes congenic
T19254 1555-1559 NNS denotes mice
T19255 1559-1560 . denotes .
R5434 T19201 T19202 npadvmod sex,specific
R5436 T19202 T19200 amod specific,phenotypes
R5437 T19203 T19202 punct -,specific
R5439 T19204 T19200 prep in,phenotypes
R5440 T19205 T19206 compound HG11,mice
R5441 T19206 T19204 pobj mice,in
R5443 T19207 T19208 mark since,is
R5444 T19208 T19192 advcl is,explain
R5446 T19209 T19208 nsubj it,is
R5447 T19210 T19211 det the,factor
R5448 T19211 T19208 attr factor,is
R5450 T19212 T19211 amod primary,factor
R5451 T19213 T19211 compound transcription,factor
R5452 T19214 T19211 amod responsible,factor
R5454 T19215 T19214 prep for,responsible
R5455 T19216 T19217 npadvmod Gh,induced
R5456 T19217 T19218 amod induced,expression
R5458 T19218 T19215 pobj expression,for
R5459 T19219 T19220 npadvmod sex,specific
R5460 T19220 T19218 amod specific,expression
R5462 T19221 T19220 punct -,specific
R5463 T19222 T19223 compound liver,gene
R5465 T19223 T19218 compound gene,expression
R5466 T19224 T19225 punct [,44
R5467 T19225 T19192 parataxis 44,explain
R5469 T19226 T19225 punct ],44
R5470 T19227 T19192 punct .,explain
R5472 T19229 T19230 amod Future,studies
R5473 T19230 T19231 nsubj studies,include
R5474 T19232 T19230 acl aimed,studies
R5475 T19233 T19232 prep at,aimed
R5476 T19234 T19233 pcomp identifying,at
R5477 T19235 T19236 det the,QTG
R5478 T19236 T19234 dobj QTG,identifying
R5479 T19237 T19236 compound HG11,QTG
R5480 T19238 T19231 punct ", ",include
R5481 T19239 T19231 aux will,include
R5482 T19240 T19231 advmod certainly,include
R5483 T19241 T19242 det a,characterization
R5485 T19242 T19231 dobj characterization,include
R5486 T19243 T19242 amod thorough,characterization
R5487 T19244 T19242 prep of,characterization
R5488 T19245 T19246 nmod Gh,patterns
R5490 T19246 T19244 pobj patterns,of
R5491 T19247 T19245 cc and,Gh
R5492 T19248 T19245 conj Stat5b,Gh
R5493 T19249 T19246 nmod sequence,patterns
R5495 T19250 T19249 cc and,sequence
R5496 T19251 T19249 conj expression,sequence
R5498 T19252 T19246 prep in,patterns
R5499 T19253 T19254 amod congenic,mice
R5500 T19254 T19252 pobj mice,in
R5502 T19255 T19231 punct .,include
R5611 T18970 T18971 det The,strain
R5616 T18971 T18973 nsubj strain,is
R5618 T18972 T18971 compound HG11,strain
R5621 T18974 T18973 prep of,is
R5626 T18975 T18976 amod particular,interest
R5629 T18976 T18974 pobj interest,of
R5636 T18977 T18973 prep for,is
R5640 T18978 T18979 det a,number
R5643 T18979 T18977 pobj number,for
R5646 T18980 T18979 prep of,number
R5647 T18981 T18980 pobj reasons,of
R5648 T18982 T18973 punct .,is
R5649 T18984 T18985 advmod First,demonstrated
R5651 T18986 T18985 punct ", ",demonstrated
R5655 T18987 T18988 npadvmod HG11,congenic
R5657 T18988 T18989 amod congenic,mice
R5658 T18989 T18985 nsubj mice,demonstrated
R5661 T18990 T18991 amod significant,interactions
R5664 T18991 T18985 dobj interactions,demonstrated
R5668 T18992 T18991 nmod strain,interactions
R5671 T18993 T18992 prep by,strain
R5675 T18994 T18993 pobj sex,by
R5678 T18995 T18985 prep for,demonstrated
R5681 T18996 T18997 det a,number
R5687 T18997 T18995 pobj number,for
R5691 T18998 T18997 prep of,number
R5695 T18999 T18998 pobj traits,of
R5697 T19000 T18985 punct .,demonstrated
R5700 T19002 T19003 nsubj Males,were
R5704 T19004 T19005 advmod generally,larger
R5709 T19005 T19003 acomp larger,were
R5713 T19006 T19005 punct ", ",larger
R5717 T19007 T19008 amod faster,growing
R5719 T19008 T19005 conj growing,larger
R5723 T19009 T19008 cc and,growing
R5726 T19010 T19008 conj longer,growing
R5730 T19011 T19003 cc and,were
R5733 T19012 T19013 det the,converse
R5740 T19013 T19014 nsubjpass converse,seen
R5744 T19014 T19003 conj seen,were
R5755 T19015 T19014 auxpass was,seen
R5757 T19016 T19014 prep in,seen
R5758 T19017 T19016 pobj females,in
R5759 T19018 T19014 punct .,seen
R5760 T19020 T19021 det The,effects
R5762 T19021 T19023 nsubj effects,are
R5766 T19022 T19021 amod confounding,effects
R5769 T19024 T19021 prep of,effects
R5774 T19025 T19024 pobj sex,of
R5778 T19026 T19023 advmod likely,are
R5781 T19027 T19028 det the,reason
R5783 T19028 T19023 attr reason,are
R5787 T19029 T19028 prep for,reason
R5794 T19030 T19031 det the,discrepancies
R5796 T19031 T19029 pobj discrepancies,for
R5797 T19032 T19031 prep between,discrepancies
R5801 T19033 T19034 det the,results
R5804 T19034 T19032 pobj results,between
R5808 T19035 T19036 amod congenic,genome
R5811 T19036 T19038 compound genome,scan
R5814 T19037 T19036 cc and,genome
R5819 T19038 T19034 compound scan,results
R5822 T19039 T19034 punct ", ",results
R5826 T19040 T19041 advmod where,analyzed
R5829 T19041 T19034 relcl analyzed,results
R5832 T19042 T19043 det both,sexes
R5835 T19043 T19041 nsubjpass sexes,analyzed
R5839 T19044 T19041 auxpass were,analyzed
R5846 T19045 T19041 advmod together,analyzed
R5850 T19046 T19023 punct .,are
R5853 T19048 T19049 advmod Secondly,found
R5857 T19050 T19049 punct ", ",found
R5862 T19051 T19049 nsubjpass Carp2,found
R5865 T19052 T19049 auxpass was,found
R5869 T19053 T19054 aux to,interact
R5872 T19054 T19049 xcomp interact,found
R5873 T19055 T19054 prep with,interact
R5874 T19056 T19055 pobj hg,with
R5875 T19057 T19049 cc and,found
R5876 T19058 T19059 nsubjpass MMU11,saturated
R5879 T19059 T19049 conj saturated,found
R5880 T19060 T19059 auxpass is,saturated
R5881 T19061 T19059 prep with,saturated
R5882 T19062 T19061 pobj genes,with
R5883 T19063 T19062 acl involved,genes
R5885 T19064 T19063 prep in,involved
R5888 T19065 T19066 det the,pathway
R5891 T19066 T19064 pobj pathway,in
R5897 T19067 T19066 amod central,pathway
R5901 T19068 T19066 nmod Gh,pathway
R5904 T19069 T19066 amod intracellular,pathway
R5908 T19070 T19066 compound signaling,pathway
R5911 T19071 T19062 punct ", ",genes
R5913 T19072 T19073 amod such,as
R5916 T19073 T19062 prep as,genes
R5920 T19074 T19073 pobj Gh,as
R5921 T19075 T19074 punct ", ",Gh
R5922 T19076 T19074 conj Stat5b,Gh
R5923 T19077 T19076 cc and,Stat5b
R5926 T19078 T19076 conj Stat5a,Stat5b
R5930 T19079 T19049 punct .,found
R5934 T19081 T19082 advmod Thirdly,identified
R5938 T19083 T19082 punct ", ",identified
R5943 T19084 T19085 compound MMU11,QTL
R5946 T19085 T19082 nsubjpass QTL,identified
R5949 T19086 T19085 compound growth,QTL
R5952 T19087 T19085 acl overlapping,QTL
R5955 T19088 T19087 dobj HG11,overlapping
R5959 T19089 T19082 aux have,identified
R5962 T19090 T19082 auxpass been,identified
R5965 T19091 T19082 prep in,identified
R5968 T19092 T19093 det a,number
R5972 T19093 T19091 pobj number,in
R5976 T19094 T19093 prep of,number
R5980 T19095 T19094 pobj crosses,of
R5983 T19096 T19082 advcl using,identified
R5985 T19097 T19098 amod different,strains
R5988 T19098 T19096 dobj strains,using
R5992 T19099 T19098 compound mouse,strains
R5995 T19100 T19101 punct [,37
R6000 T19101 T19082 parataxis 37,identified
R6001 T19102 T19103 punct -,41
R6007 T19103 T19101 prep 41,37
R6011 T19104 T19101 punct ],37
R6013 T19105 T19082 punct .,identified
R6016 T19107 T19108 advcl Given,is
R6021 T19109 T19110 det the,nature
R6026 T19110 T19107 dobj nature,Given
R6029 T19111 T19112 advmod well,documented
R6033 T19112 T19110 amod documented,nature
R6037 T19113 T19114 advmod sexually,dimorphic
R6040 T19114 T19110 amod dimorphic,nature
R6044 T19115 T19110 prep of,nature
R6047 T19116 T19117 compound Gh,secretion
R6054 T19117 T19115 pobj secretion,of
R6057 T19118 T19117 cc and,secretion
R6060 T19119 T19120 npadvmod Gh,induced
R6062 T19120 T19121 amod induced,expression
R6066 T19121 T19117 conj expression,secretion
R6070 T19122 T19121 compound gene,expression
R6073 T19123 T19124 punct [,43
R6077 T19124 T19107 parataxis 43,Given
R6080 T19125 T19124 nummod 42,43
R6083 T19126 T19124 punct ",",43
R6084 T19127 T19124 punct ],43
R6087 T19128 T19108 punct ", ",is
R6091 T19129 T19108 nsubj it,is
R6094 T19130 T19108 acomp probable,is
R6098 T19131 T19132 mark that,reside
R6102 T19132 T19108 ccomp reside,is
R6105 T19133 T19134 det the,mutation
R6108 T19134 T19132 nsubj mutation,reside
R6110 T19135 T19134 amod underlying,mutation
R6111 T19136 T19134 prep in,mutation
R6113 T19137 T19138 det the,HG11
R6116 T19138 T19136 pobj HG11,in
R6119 T19139 T19138 amod congenic,HG11
R6123 T19140 T19132 aux may,reside
R6126 T19141 T19132 prep in,reside
R6132 T19142 T19143 det a,gene
R6137 T19143 T19141 pobj gene,in
R6138 T19144 T19143 acl enhancing,gene
R6139 T19145 T19146 npadvmod Gh,induced
R6140 T19146 T19147 amod induced,effects
R6141 T19147 T19144 dobj effects,enhancing
R6142 T19148 T19149 npadvmod sex,specific
R6143 T19149 T19147 amod specific,effects
R6144 T19150 T19149 punct -,specific
R6145 T19151 T19108 punct .,is
R6146 T19153 T19154 det The,gene
R6147 T19154 T19157 nsubj gene,are
R6148 T19155 T19154 amod structural,gene
R6149 T19156 T19154 compound Gh,gene
R6150 T19158 T19154 appos itself,gene
R6151 T19159 T19154 cc and,gene
R6152 T19160 T19154 conj Stat5b,gene
R6153 T19161 T19162 amod excellent,candidates
R6154 T19162 T19157 attr candidates,are
R6155 T19163 T19157 punct .,are
R6156 T19165 T19166 det The,role
R6157 T19166 T19168 nsubj role,include
R6158 T19167 T19166 amod potential,role
R6159 T19169 T19166 prep of,role
R6160 T19170 T19169 pobj Gh,of
R6161 T19171 T19168 aux would,include
R6162 T19172 T19168 dobj polymorphism,include
R6163 T19173 T19174 dep that,alters
R6164 T19174 T19172 advcl alters,polymorphism
R6165 T19175 T19176 compound protein,function
R6166 T19176 T19174 dobj function,alters
R6167 T19177 T19174 prep in,alters
R6168 T19178 T19179 det the,absence
R6169 T19179 T19177 pobj absence,in
R6170 T19180 T19179 prep of,absence
R6171 T19181 T19180 pobj Socs2,of
R6172 T19182 T19174 cc or,alters
R6173 T19183 T19184 dep that,causes
R6174 T19184 T19174 conj causes,alters
R6175 T19185 T19186 amod transcriptional,deregulation
R6176 T19186 T19184 dobj deregulation,causes
R6177 T19187 T19186 prep of,deregulation
R6178 T19188 T19187 pobj Gh,of
R6179 T19189 T19168 punct .,include
R6180 T19191 T19192 advmod Additionally,explain
R6181 T19193 T19192 punct ", ",explain
R6182 T19194 T19195 amod functional,variation
R6183 T19195 T19192 nsubj variation,explain
R6184 T19196 T19195 prep in,variation
R6185 T19197 T19196 pobj Stat5b,in
R6186 T19198 T19192 aux may,explain
R6187 T19199 T19200 det the,phenotypes
R6188 T19200 T19192 dobj phenotypes,explain

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
T17600 88-92 NCBITaxon:10088 denotes mice
T17601 169-174 PATO_UBERON_EXT:male_or_bearer_of_maleness denotes Males
T17602 205-212 GO:0040007 denotes growing
T17603 253-260 PATO_UBERON_EXT:female_or_bearer_of_femaleness denotes females
T17604 362-368 SO_EXT:0001026 denotes genome
T17605 498-503 SO_EXT:0000704 denotes genes
T17606 528-530 CHEBI_GO_PR_EXT:growth_hormone denotes Gh
T17607 528-530 _FRAGMENT denotes Gh
T17608 545-562 GO:0060396 denotes signaling pathway
T17609 531-544 GO:0005622 denotes intracellular
T17610 531-562 GO:0030522 denotes intracellular signaling pathway
T17611 536-544 CL_GO_EXT:cell denotes cellular
T17612 572-574 CHEBI_GO_PR_EXT:growth_hormone denotes Gh
T17613 576-582 PR_EXT:000002092 denotes Stat5b
T17614 587-593 PR_EXT:000002091 denotes Stat5a
T17615 610-616 GO_EXT:biological_growth_entity_or_process denotes growth
T17616 617-620 SO_EXT:0000771 denotes QTL
T17617 698-703 NCBITaxon:10088 denotes mouse
T17618 776-778 CHEBI_GO_PR_EXT:growth_hormone denotes Gh
T17619 779-788 GO_EXT:secretion_entity_or_process denotes secretion
T17620 793-795 CHEBI_GO_PR_EXT:growth_hormone denotes Gh
T17621 804-808 SO_EXT:0000704 denotes gene
T17622 804-819 GO:0010467 denotes gene expression
T17623 864-872 SO_EXT:sequence_alteration_entity_or_process denotes mutation
T17624 910-914 SO_EXT:0000704 denotes gene
T17625 925-927 CHEBI_GO_PR_EXT:growth_hormone denotes Gh
T17626 973-975 CHEBI_GO_PR_EXT:growth_hormone denotes Gh
T17627 976-980 SO_EXT:0000704 denotes gene
T17628 992-998 PR_EXT:000002092 denotes Stat5b
T17629 1047-1049 CHEBI_GO_PR_EXT:growth_hormone denotes Gh
T17630 1064-1076 SO_EXT:polymorphism denotes polymorphism
T17631 1089-1096 CHEBI_PR_EXT:protein denotes protein
T17632 1124-1129 PR_EXT:000015393 denotes Socs2
T17633 1145-1160 GO_EXT:transcription denotes transcriptional
T17634 1163-1173 GO:0065007 denotes regulation
T17635 1177-1179 CHEBI_GO_PR_EXT:growth_hormone denotes Gh
T17636 1219-1225 PR_EXT:000002092 denotes Stat5b
T17637 1274-1278 NCBITaxon:10088 denotes mice
T17638 1303-1316 GO_EXT:transcription denotes transcription
T17639 1303-1323 GO_EXT:transcription_factor denotes transcription factor
T17640 1340-1342 CHEBI_GO_PR_EXT:growth_hormone denotes Gh
T17641 1364-1369 UBERON:0002107 denotes liver
T17642 1370-1374 SO_EXT:0000704 denotes gene
T17643 1370-1385 GO:0010467 denotes gene expression
T17644 1496-1498 CHEBI_GO_PR_EXT:growth_hormone denotes Gh
T17645 1503-1509 PR_EXT:000002092 denotes Stat5b
T17646 1510-1518 SO_EXT:biological_sequence denotes sequence
T17647 1523-1533 GO:0010467 denotes expression
T17648 1555-1559 NCBITaxon:10088 denotes mice
R4336 T17608 T17607 _lexicallyChainedTo signaling pathway,Gh

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
T17404 88-92 NCBITaxon:10088 denotes mice
T17405 205-212 GO:0040007 denotes growing
T17406 362-368 SO:0001026 denotes genome
T17407 498-503 SO:0000704 denotes genes
T17408 528-530 _FRAGMENT denotes Gh
T17409 545-562 GO:0060396 denotes signaling pathway
T17410 531-544 GO:0005622 denotes intracellular
T17411 531-562 GO:0030522 denotes intracellular signaling pathway
T17412 576-582 PR:000002092 denotes Stat5b
T17413 587-593 PR:000002091 denotes Stat5a
T17414 617-620 SO:0000771 denotes QTL
T17415 698-703 NCBITaxon:10088 denotes mouse
T17416 804-808 SO:0000704 denotes gene
T17417 804-819 GO:0010467 denotes gene expression
T17418 910-914 SO:0000704 denotes gene
T17419 976-980 SO:0000704 denotes gene
T17420 992-998 PR:000002092 denotes Stat5b
T17421 1124-1129 PR:000015393 denotes Socs2
T17422 1163-1173 GO:0065007 denotes regulation
T17423 1219-1225 PR:000002092 denotes Stat5b
T17424 1274-1278 NCBITaxon:10088 denotes mice
T17425 1364-1369 UBERON:0002107 denotes liver
T17426 1370-1374 SO:0000704 denotes gene
T17427 1370-1385 GO:0010467 denotes gene expression
T17428 1503-1509 PR:000002092 denotes Stat5b
T17429 1523-1533 GO:0010467 denotes expression
T17430 1555-1559 NCBITaxon:10088 denotes mice
R4335 T17409 T17408 _lexicallyChainedTo signaling pathway,Gh