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PubMed:19521089 JSONTXT

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TEST-DiseaseOrPhenotypicFeature

Id Subject Object Predicate Lexical cue #label
T1 87-106 DiseaseOrPhenotypicFeature denotes Parkinson's disease D010300
T2 117-136 DiseaseOrPhenotypicFeature denotes Parkinson's disease D010300
T3 138-140 DiseaseOrPhenotypicFeature denotes PD D010300
T4 147-173 DiseaseOrPhenotypicFeature denotes neurodegenerative disorder D019636
T5 182-199 DiseaseOrPhenotypicFeature denotes muscular rigidity D009127
T6 201-215 DiseaseOrPhenotypicFeature denotes resting tremor D014202
T7 220-232 DiseaseOrPhenotypicFeature denotes bradykinesia D018476
T8 282-284 DiseaseOrPhenotypicFeature denotes PD D010300
T9 621-623 DiseaseOrPhenotypicFeature denotes PD D010300
T10 701-703 DiseaseOrPhenotypicFeature denotes PD D010300
T11 845-847 DiseaseOrPhenotypicFeature denotes PD D010300
T12 963-965 DiseaseOrPhenotypicFeature denotes PD D010300

TEST-ChemicalEntity

Id Subject Object Predicate Lexical cue ID:
T1 0-9 ChemicalEntity denotes Serotonin http://purl.obolibrary.org/obo/CHEBI_28790
T2 321-330 ChemicalEntity denotes serotonin D012701|http://purl.obolibrary.org/obo/CHEBI_350546|http://purl.obolibrary.org/obo/CHEBI_28790

Test-SequenceVariant

Id Subject Object Predicate Lexical cue
T1 544-551 SequenceVariant denotes rs25531
T2 552-557 SequenceVariant denotes A-->G
T3 771-778 SequenceVariant denotes rs25531
T4 806-813 SequenceVariant denotes rs25531

Test-GeneOrGeneProduct

Id Subject Object Predicate Lexical cue
T1 0-21 GeneOrGeneProduct denotes Serotonin transporter
T2 47-55 GeneOrGeneProduct denotes 5-HTTLPR
T3 209-215 GeneOrGeneProduct denotes tremor
T4 321-342 GeneOrGeneProduct denotes serotonin transporter
T5 349-355 GeneOrGeneProduct denotes SLC6A4
T6 376-384 GeneOrGeneProduct denotes 5-HTTLPR
T7 469-484 GeneOrGeneProduct denotes SLC6A4 promoter
T8 497-512 GeneOrGeneProduct denotes SLC6A4 promoter
T9 591-594 GeneOrGeneProduct denotes 837
T10 667-675 GeneOrGeneProduct denotes 5-HTTLPR
T11 797-805 GeneOrGeneProduct denotes 5-HTTLPR
T12 876-884 GeneOrGeneProduct denotes 5-HTTLPR
T13 916-931 GeneOrGeneProduct denotes SLC6A4 promoter

Test-merged-2

Id Subject Object Predicate Lexical cue #label ID:
T89735 544-551 SequenceVariant denotes rs25531
T93545 552-557 SequenceVariant denotes A-->G
T15902 771-778 SequenceVariant denotes rs25531
T75917 806-813 SequenceVariant denotes rs25531
T78489 0-9 ChemicalEntity denotes Serotonin http://purl.obolibrary.org/obo/CHEBI_28790
T22412 321-330 ChemicalEntity denotes serotonin D012701|http://purl.obolibrary.org/obo/CHEBI_350546|http://purl.obolibrary.org/obo/CHEBI_28790
T18967 0-21 GeneOrGeneProduct denotes Serotonin transporter
T28357 47-55 GeneOrGeneProduct denotes 5-HTTLPR
T42916 209-215 GeneOrGeneProduct denotes tremor
T2527 321-342 GeneOrGeneProduct denotes serotonin transporter
T45845 349-355 GeneOrGeneProduct denotes SLC6A4
T25124 376-384 GeneOrGeneProduct denotes 5-HTTLPR
T21311 469-484 GeneOrGeneProduct denotes SLC6A4 promoter
T63274 497-512 GeneOrGeneProduct denotes SLC6A4 promoter
T85563 591-594 GeneOrGeneProduct denotes 837
T29594 667-675 GeneOrGeneProduct denotes 5-HTTLPR
T73672 797-805 GeneOrGeneProduct denotes 5-HTTLPR
T32674 876-884 GeneOrGeneProduct denotes 5-HTTLPR
T13 916-931 GeneOrGeneProduct denotes SLC6A4 promoter
T1 87-106 DiseaseOrPhenotypicFeature denotes Parkinson's disease D010300
T2 117-136 DiseaseOrPhenotypicFeature denotes Parkinson's disease D010300
T3 138-140 DiseaseOrPhenotypicFeature denotes PD D010300
T4 147-173 DiseaseOrPhenotypicFeature denotes neurodegenerative disorder D019636
T5 182-199 DiseaseOrPhenotypicFeature denotes muscular rigidity D009127
T6 201-215 DiseaseOrPhenotypicFeature denotes resting tremor D014202
T7 220-232 DiseaseOrPhenotypicFeature denotes bradykinesia D018476
T8 282-284 DiseaseOrPhenotypicFeature denotes PD D010300
T9 621-623 DiseaseOrPhenotypicFeature denotes PD D010300
T10 701-703 DiseaseOrPhenotypicFeature denotes PD D010300
T11 845-847 DiseaseOrPhenotypicFeature denotes PD D010300
T12 963-965 DiseaseOrPhenotypicFeature denotes PD D010300

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 544-551 SNP:rs25531 denotes rs25531
T2 552-557 DNAMutation:|SUB|A||G denotes A-->G
T3 771-778 SNP:rs25531 denotes rs25531
T4 806-813 SNP:rs25531 denotes rs25531