> top > docs > PubMed:15086325 > annotations

PubMed:15086325 JSONTXT

Annnotations TAB JSON ListView MergeView

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
698 24-26 GeneOrGeneProduct denotes F5 NCBIGene:2153
699 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency MESH:D005166
700 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency MESH:D005166
701 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency MESH:D005166
702 387-389 GeneOrGeneProduct denotes FV NCBIGene:2153
703 456-458 GeneOrGeneProduct denotes F5 NCBIGene:2153
704 712-722 SequenceVariant denotes IVS8 -2A>G c|SUB|A|IVS8-2|G
705 745-747 GeneOrGeneProduct denotes F5 NCBIGene:2153
706 952-1001 SequenceVariant denotes insertion introduced eight additional amino acids p|INS||8
707 1016-1018 GeneOrGeneProduct denotes FV NCBIGene:2153
708 1058-1060 GeneOrGeneProduct denotes F5 NCBIGene:2153
709 1100-1112 SequenceVariant denotes 2238-9del AG c|DEL|2238_2239|AG
710 1167-1173 SequenceVariant denotes 689 AA c|Allele|A|689
711 1198-1208 SequenceVariant denotes G6410 by T g|SUB|G|6410|T
712 1250-1260 SequenceVariant denotes Gly2079Val p|SUB|G|2079|V
713 1268-1270 GeneOrGeneProduct denotes F5 NCBIGene:2153
714 1287-1297 SequenceVariant denotes IVS8 -2A>G c|SUB|A|IVS8-2|G
715 1299-1311 SequenceVariant denotes 2238-9del AG c|DEL|2238_2239|AG
716 1316-1322 SequenceVariant denotes G6410T g|SUB|G|6410|T
717 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency MESH:D005166

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-125 Sentence denotes Identification of three F5 gene mutations associated with inherited coagulation factor V deficiency in two Chinese pedigrees.
T2 126-228 Sentence denotes To investigate the molecular defects in two Chinese pedigrees with inherited factor V (FV) deficiency.
T3 229-411 Sentence denotes A 37-year-old male (proband 1) and an 18-month-old boy (proband 2) were diagnosed as inherited coagulation FV deficiency by severely reduced plasma levels of FV activity and antigen.
T4 412-577 Sentence denotes All 25 exons and their flanking sequence of F5 gene were amplified by polymerase chain reaction (PCR) for both probands and the PCR products were directly sequenced.
T5 578-687 Sentence denotes Total RNA was extracted from the peripheral lymphocytes of proband 1 for detecting the changes at mRNA level.
T6 688-947 Sentence denotes The homozygous deletion IVS8 -2A>G was identified in the F5 gene of proband 1 and complementary DNA (cDNA) analysis revealed the abolishment of the canonical splicing site by the mutation and the activation of the cryptic acceptor site 24 bp upstream instead.
T7 948-1027 Sentence denotes The insertion introduced eight additional amino acids (AA) into the FV protein.
T8 1028-1095 Sentence denotes Two heterozygous mutations of F5 gene were discovered in proband 2.
T9 1096-1261 Sentence denotes The 2238-9del AG in exon 13 introduced a premature termination code at 689 AA and the substitution of G6410 by T in exon 23 lead to the missense mutation Gly2079Val.
T10 1262-1413 Sentence denotes Three F5 gene mutations, IVS8 -2A>G, 2238-9del AG and G6410T, have been identified in two Chinese pedigree with congenital FV deficiency, respectively.

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 58-67 DiseaseOrPhenotypicFeature denotes inherited 0021152
T2 80-99 DiseaseOrPhenotypicFeature denotes factor V deficiency 0020586
T3 193-202 DiseaseOrPhenotypicFeature denotes inherited 0021152
T4 314-323 DiseaseOrPhenotypicFeature denotes inherited 0021152
T5 1374-1384 DiseaseOrPhenotypicFeature denotes congenital 0021140

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T1 1100-1112 SequenceVariant denotes 2238-9del AG
T2 1198-1208 SequenceVariant denotes G6410 by T
T3 1250-1260 SequenceVariant denotes Gly2079Val
T4 1299-1311 SequenceVariant denotes 2238-9del AG
T5 1316-1322 SequenceVariant denotes G6410T

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 32-41 GeneOrGeneProduct denotes mutations
T2 68-88 GeneOrGeneProduct denotes coagulation factor V
T3 155-162 GeneOrGeneProduct denotes defects
T4 203-209 GeneOrGeneProduct denotes factor
T5 234-238 GeneOrGeneProduct denotes year
T6 243-247 GeneOrGeneProduct denotes male
T7 264-269 GeneOrGeneProduct denotes an 18
T8 362-369 GeneOrGeneProduct denotes reduced
T9 390-398 GeneOrGeneProduct denotes activity
T10 403-410 GeneOrGeneProduct denotes antigen
T11 412-415 GeneOrGeneProduct denotes All
T12 482-492 GeneOrGeneProduct denotes polymerase
T13 493-498 GeneOrGeneProduct denotes chain
T14 544-552 GeneOrGeneProduct denotes products
T15 578-583 GeneOrGeneProduct denotes Total
T16 622-633 GeneOrGeneProduct denotes lymphocytes
T17 676-680 GeneOrGeneProduct denotes mRNA
T18 764-769 GeneOrGeneProduct denotes 1 and
T19 789-793 GeneOrGeneProduct denotes cDNA
T20 846-854 GeneOrGeneProduct denotes splicing
T21 867-875 GeneOrGeneProduct denotes mutation
T22 884-894 GeneOrGeneProduct denotes activation
T23 902-909 GeneOrGeneProduct denotes cryptic
T24 990-1001 GeneOrGeneProduct denotes amino acids
T25 1003-1005 GeneOrGeneProduct denotes AA
T26 1019-1026 GeneOrGeneProduct denotes protein
T27 1045-1054 GeneOrGeneProduct denotes mutations
T28 1171-1173 GeneOrGeneProduct denotes AA
T29 1232-1240 GeneOrGeneProduct denotes missense
T30 1241-1249 GeneOrGeneProduct denotes mutation
T31 1276-1285 GeneOrGeneProduct denotes mutations

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 68-88 GeneOrGeneProduct denotes coagulation factor V
T2 203-209 GeneOrGeneProduct denotes factor
T3 362-369 GeneOrGeneProduct denotes reduced
T4 403-410 GeneOrGeneProduct denotes antigen
T5 482-492 GeneOrGeneProduct denotes polymerase
T6 493-498 GeneOrGeneProduct denotes chain
T7 622-633 GeneOrGeneProduct denotes lymphocytes
T8 676-680 GeneOrGeneProduct denotes mRNA
T9 789-793 GeneOrGeneProduct denotes cDNA
T10 902-909 GeneOrGeneProduct denotes cryptic
T11 990-1001 GeneOrGeneProduct denotes amino acids
T12 1003-1005 GeneOrGeneProduct denotes AA
T13 1019-1026 GeneOrGeneProduct denotes protein
T14 1171-1173 GeneOrGeneProduct denotes AA

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 80-99 DiseaseOrPhenotypicFeature denotes factor V deficiency D005166

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 68-88 GeneOrGeneProduct denotes coagulation factor V
T2 203-211 GeneOrGeneProduct denotes factor V
T3 213-215 GeneOrGeneProduct denotes FV
T4 336-338 GeneOrGeneProduct denotes FV
T5 387-389 GeneOrGeneProduct denotes FV
T6 1016-1018 GeneOrGeneProduct denotes FV
T7 1385-1387 GeneOrGeneProduct denotes FV

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 80-99 DiseaseOrPhenotypicFeature denotes factor V deficiency 0020586|0009210

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency DISEASE
T2 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency DISEASE
T3 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency DISEASE
T4 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency DISEASE

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency DISEASE
T2 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency DISEASE
T3 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency DISEASE
T4 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency DISEASE

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 1220-1224 ChemicalEntity denotes lead D007854

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T1 1220-1224 ChemicalEntity denotes lead D007854
T7 1385-1387 GeneOrGeneProduct denotes FV
T6 1016-1018 GeneOrGeneProduct denotes FV
T5 387-389 GeneOrGeneProduct denotes FV
T4 336-338 GeneOrGeneProduct denotes FV
T3 213-215 GeneOrGeneProduct denotes FV
T2 203-211 GeneOrGeneProduct denotes factor V
T37256 68-88 GeneOrGeneProduct denotes coagulation factor V
T98511 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency DISEASE
T24581 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency DISEASE
T60595 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency DISEASE
T48743 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency DISEASE
T54016 1316-1322 SequenceVariant denotes G6410T
T52182 1299-1311 SequenceVariant denotes 2238-9del AG
T53136 1250-1260 SequenceVariant denotes Gly2079Val
T14759 1198-1208 SequenceVariant denotes G6410 by T
T42451 1100-1112 SequenceVariant denotes 2238-9del AG

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 712-722 DNAMutation:c|SUB|A|IVS8-2|G denotes IVS8 -2A>G
T2 1100-1112 DNAMutation:c|DEL|2238_2239|AG denotes 2238-9del AG
T3 1198-1208 DNAMutation:g|SUB|G|6410|T denotes G6410 by T
T4 1250-1260 ProteinMutation:p|SUB|G|2079|V denotes Gly2079Val
T5 1287-1297 DNAMutation:c|SUB|A|IVS8-2|G denotes IVS8 -2A>G
T6 1299-1311 DNAMutation:c|DEL|2238_2239|AG denotes 2238-9del AG
T7 1316-1322 DNAMutation:g|SUB|G|6410|T denotes G6410T

biored-valid

Id Subject Object Predicate Lexical cue
T1 24-26 GeneOrGeneProduct denotes F5
T2 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency
T3 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency
T4 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency
T5 387-389 GeneOrGeneProduct denotes FV
T6 456-458 GeneOrGeneProduct denotes F5
T7 712-722 SequenceVariant denotes IVS8 -2A>G
T8 745-747 GeneOrGeneProduct denotes F5
T9 952-1001 SequenceVariant denotes insertion introduced eight additional amino acids
T10 1016-1018 GeneOrGeneProduct denotes FV
T11 1058-1060 GeneOrGeneProduct denotes F5
T12 1100-1112 SequenceVariant denotes 2238-9del AG
T13 1167-1173 SequenceVariant denotes 689 AA
T14 1198-1208 SequenceVariant denotes G6410 by T
T15 1250-1260 SequenceVariant denotes Gly2079Val
T16 1268-1270 GeneOrGeneProduct denotes F5
T17 1287-1297 SequenceVariant denotes IVS8 -2A>G
T18 1299-1311 SequenceVariant denotes 2238-9del AG
T19 1316-1322 SequenceVariant denotes G6410T
T20 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-deepseek-nr-ng

Id Subject Object Predicate Lexical cue
T1 24-26 GeneOrGeneProduct denotes F5
T2 213-215 GeneOrGeneProduct denotes FV
T3 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency
T4 387-389 GeneOrGeneProduct denotes FV
T5 456-458 GeneOrGeneProduct denotes F5
T6 712-722 SequenceVariant denotes IVS8 -2A>G
T7 745-747 GeneOrGeneProduct denotes F5
T8 1016-1018 GeneOrGeneProduct denotes FV
T9 1100-1112 SequenceVariant denotes 2238-9del AG
T10 1250-1260 SequenceVariant denotes Gly2079Val
T11 1316-1322 SequenceVariant denotes G6410T
T12 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-deepseek-nr-g

Id Subject Object Predicate Lexical cue
T1 24-31 GeneOrGeneProduct denotes F5 gene
T2 80-99 DiseaseOrPhenotypicFeature denotes factor V deficiency
T3 213-227 DiseaseOrPhenotypicFeature denotes FV) deficiency
T4 336-349 DiseaseOrPhenotypicFeature denotes FV deficiency
T5 387-398 GeneOrGeneProduct denotes FV activity
T6 456-463 GeneOrGeneProduct denotes F5 gene
T7 509-512 ChemicalEntity denotes PCR
T8 540-552 ChemicalEntity denotes PCR products
T9 584-587 ChemicalEntity denotes RNA
T10 676-686 GeneOrGeneProduct denotes mRNA level
T11 712-722 SequenceVariant denotes IVS8 -2A>G
T12 745-752 GeneOrGeneProduct denotes F5 gene
T13 789-793 GeneOrGeneProduct denotes cDNA
T14 1016-1026 GeneOrGeneProduct denotes FV protein
T15 1100-1112 SequenceVariant denotes 2238-9del AG
T16 1316-1322 SequenceVariant denotes G6410T

biored-valid-deepseek-r-ng

Id Subject Object Predicate Lexical cue
T1 24-31 GeneOrGeneProduct denotes F5 gene
T2 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency
T3 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency
T4 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency
T5 387-389 GeneOrGeneProduct denotes FV
T6 456-463 GeneOrGeneProduct denotes F5 gene
T7 712-722 SequenceVariant denotes IVS8 -2A>G
T8 745-752 GeneOrGeneProduct denotes F5 gene
T9 1100-1112 SequenceVariant denotes 2238-9del AG
T10 1250-1260 SequenceVariant denotes Gly2079Val
T11 1316-1322 SequenceVariant denotes G6410T
T12 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-deepseek-r-g

Id Subject Object Predicate Lexical cue
T1 24-31 GeneOrGeneProduct denotes F5 gene
T2 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency
T3 213-215 GeneOrGeneProduct denotes FV
T4 336-349 DiseaseOrPhenotypicFeature denotes FV deficiency
T5 456-463 GeneOrGeneProduct denotes F5 gene
T6 676-680 GeneOrGeneProduct denotes mRNA
T7 712-722 SequenceVariant denotes IVS8 -2A>G
T8 789-793 GeneOrGeneProduct denotes cDNA
T9 1016-1026 GeneOrGeneProduct denotes FV protein
T10 1100-1112 SequenceVariant denotes 2238-9del AG
T11 1250-1260 SequenceVariant denotes Gly2079Val
T12 1316-1322 SequenceVariant denotes G6410T
T13 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-gemini-nr-ng

Id Subject Object Predicate Lexical cue
T1 24-26 GeneOrGeneProduct denotes F5
T2 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency
T3 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency
T4 387-389 GeneOrGeneProduct denotes FV
T5 456-458 GeneOrGeneProduct denotes F5
T6 712-722 SequenceVariant denotes IVS8 -2A>G
T7 745-747 GeneOrGeneProduct denotes F5
T8 1100-1112 SequenceVariant denotes 2238-9del AG
T9 1250-1260 SequenceVariant denotes Gly2079Val
T10 1316-1322 SequenceVariant denotes G6410T
T11 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-gemini-r-ng

Id Subject Object Predicate Lexical cue
T1 24-31 GeneOrGeneProduct denotes F5 gene
T2 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency
T3 107-114 OrganismTaxon denotes Chinese
T4 203-211 GeneOrGeneProduct denotes factor V
T5 213-215 GeneOrGeneProduct denotes FV
T6 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency
T7 456-463 GeneOrGeneProduct denotes F5 gene
T8 584-587 ChemicalEntity denotes RNA
T9 676-680 ChemicalEntity denotes mRNA
T10 712-722 SequenceVariant denotes IVS8 -2A>G
T11 745-752 GeneOrGeneProduct denotes F5 gene
T12 770-787 ChemicalEntity denotes complementary DNA
T13 789-793 ChemicalEntity denotes cDNA
T14 990-1001 ChemicalEntity denotes amino acids
T15 1003-1005 ChemicalEntity denotes AA
T16 1016-1026 GeneOrGeneProduct denotes FV protein
T17 1058-1065 GeneOrGeneProduct denotes F5 gene
T18 1100-1112 SequenceVariant denotes 2238-9del AG
T19 1250-1260 SequenceVariant denotes Gly2079Val
T20 1287-1297 SequenceVariant denotes IVS8 -2A>G
T21 1316-1322 SequenceVariant denotes G6410T
T22 1352-1359 OrganismTaxon denotes Chinese
T23 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-gemini-r-g

Id Subject Object Predicate Lexical cue
T1 24-31 GeneOrGeneProduct denotes F5 gene
T2 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency
T3 107-114 OrganismTaxon denotes Chinese
T4 203-227 DiseaseOrPhenotypicFeature denotes factor V (FV) deficiency
T5 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency
T6 456-463 GeneOrGeneProduct denotes F5 gene
T7 712-722 SequenceVariant denotes IVS8 -2A>G
T8 745-752 GeneOrGeneProduct denotes F5 gene
T9 1016-1026 GeneOrGeneProduct denotes FV protein
T10 1058-1065 GeneOrGeneProduct denotes F5 gene
T11 1100-1112 SequenceVariant denotes 2238-9del AG
T12 1250-1260 SequenceVariant denotes Gly2079Val
T13 1287-1297 SequenceVariant denotes IVS8 -2A>G
T14 1316-1322 SequenceVariant denotes G6410T
T15 1352-1359 OrganismTaxon denotes Chinese
T16 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-gpt-nr-ng

Id Subject Object Predicate Lexical cue
T1 24-31 GeneOrGeneProduct denotes F5 gene
T2 80-88 GeneOrGeneProduct denotes factor V
T3 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency
T4 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency
T5 353-411 DiseaseOrPhenotypicFeature denotes severely reduced plasma levels of FV activity and antigen.
T6 456-463 GeneOrGeneProduct denotes F5 gene
T7 578-587 ChemicalEntity denotes Total RNA
T8 676-680 ChemicalEntity denotes mRNA
T9 712-722 SequenceVariant denotes IVS8 -2A>G
T10 745-752 GeneOrGeneProduct denotes F5 gene
T11 784-787 ChemicalEntity denotes DNA
T12 789-793 ChemicalEntity denotes cDNA
T13 990-1001 ChemicalEntity denotes amino acids
T14 1016-1026 GeneOrGeneProduct denotes FV protein
T15 1058-1065 GeneOrGeneProduct denotes F5 gene
T16 1100-1112 SequenceVariant denotes 2238-9del AG
T17 1250-1260 SequenceVariant denotes Gly2079Val
T18 1268-1275 GeneOrGeneProduct denotes F5 gene
T19 1316-1322 SequenceVariant denotes G6410T
T20 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-gpt-nr-g

Id Subject Object Predicate Lexical cue
T1 24-31 GeneOrGeneProduct denotes F5 gene
T2 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency
T3 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency
T4 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency
T5 456-463 GeneOrGeneProduct denotes F5 gene
T6 712-722 SequenceVariant denotes IVS8 -2A>G
T7 745-752 GeneOrGeneProduct denotes F5 gene
T8 1016-1026 GeneOrGeneProduct denotes FV protein
T9 1058-1065 GeneOrGeneProduct denotes F5 gene
T10 1100-1112 SequenceVariant denotes 2238-9del AG
T11 1250-1260 SequenceVariant denotes Gly2079Val
T12 1268-1275 GeneOrGeneProduct denotes F5 gene
T13 1287-1297 SequenceVariant denotes IVS8 -2A>G
T14 1299-1311 SequenceVariant denotes 2238-9del AG
T15 1316-1322 SequenceVariant denotes G6410T
T16 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-gpt-r-g

Id Subject Object Predicate Lexical cue
T1 24-31 GeneOrGeneProduct denotes F5 gene
T2 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency
T3 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency
T4 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency
T5 387-389 GeneOrGeneProduct denotes FV
T6 456-463 GeneOrGeneProduct denotes F5 gene
T7 712-722 SequenceVariant denotes IVS8 -2A>G
T8 745-752 GeneOrGeneProduct denotes F5 gene
T9 1016-1026 GeneOrGeneProduct denotes FV protein
T10 1058-1065 GeneOrGeneProduct denotes F5 gene
T11 1100-1112 SequenceVariant denotes 2238-9del AG
T12 1250-1260 SequenceVariant denotes Gly2079Val
T13 1268-1275 GeneOrGeneProduct denotes F5 gene
T14 1287-1297 SequenceVariant denotes IVS8 -2A>G
T15 1299-1311 SequenceVariant denotes 2238-9del AG
T16 1316-1322 SequenceVariant denotes G6410T
T17 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-gpt-r-ng

Id Subject Object Predicate Lexical cue
T1 24-31 GeneOrGeneProduct denotes F5 gene
T2 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency
T3 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency
T4 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency
T5 387-389 GeneOrGeneProduct denotes FV
T6 456-463 GeneOrGeneProduct denotes F5 gene
T7 584-587 ChemicalEntity denotes RNA
T8 676-680 ChemicalEntity denotes mRNA
T9 712-722 SequenceVariant denotes IVS8 -2A>G
T10 745-752 GeneOrGeneProduct denotes F5 gene
T11 784-787 ChemicalEntity denotes DNA
T12 789-793 ChemicalEntity denotes cDNA
T13 990-1006 ChemicalEntity denotes amino acids (AA)
T14 1016-1026 GeneOrGeneProduct denotes FV protein
T15 1058-1065 GeneOrGeneProduct denotes F5 gene
T16 1100-1112 SequenceVariant denotes 2238-9del AG
T17 1171-1173 ChemicalEntity denotes AA
T18 1250-1260 SequenceVariant denotes Gly2079Val
T19 1268-1275 GeneOrGeneProduct denotes F5 gene
T20 1287-1297 SequenceVariant denotes IVS8 -2A>G
T21 1299-1311 SequenceVariant denotes 2238-9del AG
T22 1316-1322 SequenceVariant denotes G6410T
T23 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-gemini-nr-g

Id Subject Object Predicate Lexical cue
T1 24-26 GeneOrGeneProduct denotes F5
T2 32-41 SequenceVariant denotes mutations
T3 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency
T4 107-114 OrganismTaxon denotes Chinese
T5 193-216 DiseaseOrPhenotypicFeature denotes inherited factor V (FV)
T6 217-227 DiseaseOrPhenotypicFeature denotes deficiency
T7 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency
T8 456-458 GeneOrGeneProduct denotes F5
T9 712-722 SequenceVariant denotes IVS8 -2A>G
T10 745-747 GeneOrGeneProduct denotes F5
T11 1016-1018 GeneOrGeneProduct denotes FV
T12 1045-1054 SequenceVariant denotes mutations
T13 1058-1060 GeneOrGeneProduct denotes F5
T14 1100-1112 SequenceVariant denotes 2238-9del AG
T15 1250-1260 SequenceVariant denotes Gly2079Val
T16 1287-1297 SequenceVariant denotes IVS8 -2A>G
T17 1316-1322 SequenceVariant denotes G6410T
T18 1352-1359 OrganismTaxon denotes Chinese
T19 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-gpt-r-m

Id Subject Object Predicate Lexical cue
T1 24-31 GeneOrGeneProduct denotes F5 gene
T2 80-99 DiseaseOrPhenotypicFeature denotes factor V deficiency
T3 203-227 DiseaseOrPhenotypicFeature denotes factor V (FV) deficiency
T4 249-258 OrganismTaxon denotes proband 1
T5 285-294 OrganismTaxon denotes proband 2
T6 336-349 DiseaseOrPhenotypicFeature denotes FV deficiency
T7 387-389 GeneOrGeneProduct denotes FV
T8 456-463 GeneOrGeneProduct denotes F5 gene
T9 523-531 OrganismTaxon denotes probands
T10 637-646 OrganismTaxon denotes proband 1
T11 712-722 SequenceVariant denotes IVS8 -2A>G
T12 745-752 GeneOrGeneProduct denotes F5 gene
T13 756-765 OrganismTaxon denotes proband 1
T14 1016-1018 GeneOrGeneProduct denotes FV
T15 1058-1065 GeneOrGeneProduct denotes F5 gene
T16 1085-1094 OrganismTaxon denotes proband 2
T17 1100-1112 SequenceVariant denotes 2238-9del AG
T18 1250-1260 SequenceVariant denotes Gly2079Val
T19 1268-1275 GeneOrGeneProduct denotes F5 gene
T20 1287-1297 SequenceVariant denotes IVS8 -2A>G
T21 1299-1311 SequenceVariant denotes 2238-9del AG
T22 1316-1322 SequenceVariant denotes G6410T
T23 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-gemini-r-m

Id Subject Object Predicate Lexical cue
T1 24-26 GeneOrGeneProduct denotes F5
T2 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency
T3 107-114 OrganismTaxon denotes Chinese
T4 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency
T5 243-247 OrganismTaxon denotes male
T6 249-258 OrganismTaxon denotes proband 1
T7 280-283 OrganismTaxon denotes boy
T8 285-294 OrganismTaxon denotes proband 2
T9 314-349 DiseaseOrPhenotypicFeature denotes inherited coagulation FV deficiency
T10 456-458 GeneOrGeneProduct denotes F5
T11 523-531 OrganismTaxon denotes probands
T12 578-587 ChemicalEntity denotes Total RNA
T13 637-646 OrganismTaxon denotes proband 1
T14 676-680 ChemicalEntity denotes mRNA
T15 712-722 SequenceVariant denotes IVS8 -2A>G
T16 745-747 GeneOrGeneProduct denotes F5
T17 756-765 OrganismTaxon denotes proband 1
T18 770-794 ChemicalEntity denotes complementary DNA (cDNA)
T19 1016-1018 GeneOrGeneProduct denotes FV
T20 1058-1060 GeneOrGeneProduct denotes F5
T21 1085-1094 OrganismTaxon denotes proband 2
T22 1100-1112 SequenceVariant denotes 2238-9del AG
T23 1250-1260 SequenceVariant denotes Gly2079Val
T24 1287-1297 SequenceVariant denotes IVS8 -2A>G
T25 1316-1322 SequenceVariant denotes G6410T
T26 1352-1359 OrganismTaxon denotes Chinese
T27 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency

biored-valid-deepseek-r-m

Id Subject Object Predicate Lexical cue
T1 24-31 GeneOrGeneProduct denotes F5 gene
T2 58-99 DiseaseOrPhenotypicFeature denotes inherited coagulation factor V deficiency
T3 193-227 DiseaseOrPhenotypicFeature denotes inherited factor V (FV) deficiency
T4 584-587 GeneOrGeneProduct denotes RNA
T5 676-680 GeneOrGeneProduct denotes mRNA
T6 712-722 SequenceVariant denotes IVS8 -2A>G
T7 789-793 GeneOrGeneProduct denotes cDNA
T8 1100-1112 SequenceVariant denotes 2238-9del AG
T9 1250-1260 SequenceVariant denotes Gly2079Val
T10 1316-1322 SequenceVariant denotes G6410T
T11 1374-1398 DiseaseOrPhenotypicFeature denotes congenital FV deficiency