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PMC:1584416 / 41-340 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T90 1-3 IN denotes by
T91 4-14 JJ denotes Homozygous
T92 26-33 NNS denotes Alleles
T93 15-21 JJ denotes Lethal
T94 22-25 NN denotes Xpd
T95 83-291 sentence denotes Although compound heterozygosity, or the presence of two different mutant alleles of the same gene, is common in human recessive disease, its potential to impact disease outcome has not been well documented.
T96 84-92 IN denotes Although
T97 184-186 VBZ denotes is
T98 93-101 NN denotes compound
T99 102-116 NN denotes heterozygosity
T100 116-118 , denotes ,
T101 118-120 CC denotes or
T102 121-124 DT denotes the
T103 125-133 NN denotes presence
T104 134-136 IN denotes of
T105 137-140 CD denotes two
T106 158-165 NNS denotes alleles
T107 141-150 JJ denotes different
T108 151-157 JJ denotes mutant
T109 166-168 IN denotes of
T110 169-172 DT denotes the
T111 178-182 NN denotes gene
T112 173-177 JJ denotes same
T113 182-184 , denotes ,
T114 280-290 VBN denotes documented
T115 187-193 JJ denotes common
T116 194-196 IN denotes in
T117 197-202 JJ denotes human
T118 213-220 NN denotes disease
T119 203-212 JJ denotes recessive
T120 220-222 , denotes ,
T121 222-225 PRP$ denotes its
T122 226-235 NN denotes potential
T123 236-238 TO denotes to
T124 239-245 VB denotes impact
T125 246-253 NN denotes disease
T126 254-261 NN denotes outcome
T127 262-265 VBZ denotes has
T128 266-269 RB denotes not
T129 270-274 VBN denotes been
T130 275-279 RB denotes well
T131 290-291 . denotes .
T133 292-296 DT denotes This
T134 297-299 VBZ denotes is
R7 T92 T90 pobj Alleles,by
R8 T93 T92 amod Lethal,Alleles
R9 T94 T92 compound Xpd,Alleles
R11 T97 T114 advcl is,documented
R12 T98 T99 compound compound,heterozygosity
R13 T99 T97 nsubj heterozygosity,is
R14 T100 T99 punct ", ",heterozygosity
R15 T101 T99 cc or,heterozygosity
R16 T102 T103 det the,presence
R17 T103 T99 conj presence,heterozygosity
R18 T104 T103 prep of,presence
R19 T105 T106 nummod two,alleles
R20 T106 T104 pobj alleles,of
R21 T107 T106 amod different,alleles
R22 T108 T106 amod mutant,alleles
R23 T109 T106 prep of,alleles
R24 T110 T111 det the,gene
R26 T112 T111 amod same,gene
R27 T113 T97 punct ", ",is
R31 T118 T116 pobj disease,in
R32 T119 T118 amod recessive,disease
R34 T121 T122 poss its,potential
R6 T91 T92 amod Homozygous,Alleles
R10 T96 T97 mark Although,is
R25 T111 T109 pobj gene,of
R28 T115 T97 acomp common,is
R29 T116 T97 prep in,is
R30 T117 T118 amod human,disease
R33 T120 T114 punct ", ",documented
R35 T122 T114 nsubjpass potential,documented
R36 T123 T124 aux to,impact
R37 T124 T122 acl impact,potential
R38 T125 T126 compound disease,outcome
R39 T126 T124 dobj outcome,impact
R40 T127 T114 aux has,documented
R41 T128 T114 neg not,documented
R42 T129 T114 auxpass been,documented
R43 T130 T114 advmod well,documented
R44 T131 T114 punct .,documented
R45 T133 T134 nsubj This,is

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
T20 22-25 PR:000007164 denotes Xpd
T21 26-33 SO:0001023 denotes Alleles
T22 158-165 SO:0001023 denotes alleles
T23 178-182 SO:0000704 denotes gene
T24 197-202 NCBITaxon:9606 denotes human

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
T48 15-21 GO_EXT:fatality_or_lethality denotes Lethal
T49 22-25 PR_EXT:000007164 denotes Xpd
T50 26-33 SO_EXT:0001023 denotes Alleles
T51 151-157 SO_EXT:sequence_altered_entity_or_alteration_process denotes mutant
T52 158-165 SO_EXT:0001023 denotes alleles
T53 178-182 SO_EXT:0000704 denotes gene
T54 197-202 NCBITaxon:9606 denotes human