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PMC:1584416 / 123-261 JSONTXT 4 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T96 2-10 IN denotes Although
T98 11-19 NN denotes compound
T99 20-34 NN denotes heterozygosity
T100 34-36 , denotes ,
T101 36-38 CC denotes or
T102 39-42 DT denotes the
T103 43-51 NN denotes presence
T104 52-54 IN denotes of
T105 55-58 CD denotes two
T107 59-68 JJ denotes different
T108 69-75 JJ denotes mutant
T106 76-83 NNS denotes alleles
T109 84-86 IN denotes of
T110 87-90 DT denotes the
T112 91-95 JJ denotes same
T111 96-100 NN denotes gene
T113 100-102 , denotes ,
T97 102-104 VBZ denotes is
T115 105-111 JJ denotes common
T116 112-114 IN denotes in
T117 115-120 JJ denotes human
T119 121-130 JJ denotes recessive
T118 131-138 NN denotes disease
R10 T96 T97 mark Although,is
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
R25 T111 T109 pobj gene,of
R26 T112 T111 amod same,gene
R27 T113 T97 punct ", ",is
R28 T115 T97 acomp common,is
R29 T116 T97 prep in,is
R30 T117 T118 amod human,disease
R31 T118 T116 pobj disease,in
R32 T119 T118 amod recessive,disease