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PMC:1892049 / 2737-2913 JSONTXT

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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
T1465 56-63 SO_EXT:0000704 denotes genetic
T1466 87-95 GO_EXT:biological_movement_or_translocation_process denotes movement
T1467 157-165 SO_EXT:sequence_alteration_entity_or_process denotes mutation
T1468 169-175 NCBITaxon:9606 denotes humans

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
T1450 56-63 SO:0000704 denotes genetic
T1451 169-175 NCBITaxon:9606 denotes humans

craft-sa-dev

Id Subject Object Predicate Lexical cue
T1577 0-176 sentence denotes We embarked on a series of experiments to identify the genetic lesion underlying this movement disorder and to identify a cognate disease and corresponding mutation in humans.
T1578 1-3 PRP denotes We
T1579 4-12 VBD denotes embarked
T1580 13-15 IN denotes on
T1581 16-17 DT denotes a
T1582 18-24 NN denotes series
T1583 25-27 IN denotes of
T1584 28-39 NNS denotes experiments
T1585 40-42 TO denotes to
T1586 43-51 VB denotes identify
T1587 52-55 DT denotes the
T1588 64-70 NN denotes lesion
T1589 56-63 JJ denotes genetic
T1590 71-81 VBG denotes underlying
T1591 82-86 DT denotes this
T1592 96-104 NN denotes disorder
T1593 87-95 NN denotes movement
T1594 105-108 CC denotes and
T1595 109-111 TO denotes to
T1596 112-120 VB denotes identify
T1597 121-122 DT denotes a
T1598 131-138 NN denotes disease
T1599 123-130 JJ denotes cognate
T1600 139-142 CC denotes and
T1601 143-156 VBG denotes corresponding
T1602 157-165 NN denotes mutation
T1603 166-168 IN denotes in
T1604 169-175 NNS denotes humans
T1605 175-176 . denotes .
R338 T1578 T1579 nsubj We,embarked
R339 T1580 T1579 prep on,embarked
R340 T1581 T1582 det a,series
R341 T1582 T1580 pobj series,on
R342 T1583 T1582 prep of,series
R343 T1584 T1583 pobj experiments,of
R344 T1585 T1586 aux to,identify
R345 T1586 T1579 advcl identify,embarked
R346 T1587 T1588 det the,lesion
R347 T1588 T1586 dobj lesion,identify
R348 T1589 T1588 amod genetic,lesion
R349 T1590 T1588 acl underlying,lesion
R350 T1591 T1592 det this,disorder
R351 T1592 T1590 dobj disorder,underlying
R352 T1593 T1592 compound movement,disorder
R353 T1594 T1586 cc and,identify
R354 T1595 T1596 aux to,identify
R355 T1596 T1586 conj identify,identify
R356 T1597 T1598 det a,disease
R357 T1598 T1596 dobj disease,identify
R358 T1599 T1598 amod cognate,disease
R359 T1600 T1598 cc and,disease
R360 T1601 T1602 amod corresponding,mutation
R361 T1602 T1598 conj mutation,disease
R362 T1603 T1596 prep in,identify
R363 T1604 T1603 pobj humans,in
R364 T1605 T1579 punct .,embarked