PubMed:15241482 / 1375-1648
Annnotations
LitCoin-entities
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
978 | 32-36 | GeneOrGeneProduct | denotes | PON1 | NCBIGene:5444 |
979 | 37-42 | SequenceVariant | denotes | 192RR | p|Allele|R|192 |
980 | 98-103 | OrganismTaxon | denotes | women | NCBITaxon:9606 |
981 | 188-191 | DiseaseOrPhenotypicFeature | denotes | CHD | MESH:D003327 |
982 | 220-223 | DiseaseOrPhenotypicFeature | denotes | CHD | MESH:D003327 |
983 | 269-272 | DiseaseOrPhenotypicFeature | denotes | CHD | MESH:D003327 |
LitCoin-sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T12 | 0-273 | Sentence | denotes | Our results thus indicates that PON1 192RR homozygosity is associated with increased mortality in women in the second half of life and that this increased mortality is possibly related to CHD severity and survival after CHD rather than susceptibility to development of CHD. |
LitCoin-SeqVar
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T7 | 37-42 | SequenceVariant | denotes | 192RR |
LitCoin-GeneOrGeneProduct-v0
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T17 | 32-36 | GeneOrGeneProduct | denotes | PON1 |
T18 | 118-130 | GeneOrGeneProduct | denotes | half of life |
LitCoin-GeneOrGeneProduct-v2
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T11 | 32-36 | GeneOrGeneProduct | denotes | PON1 |
LitCoin-Disease-MeSH
Id | Subject | Object | Predicate | Lexical cue | originalLabel |
---|---|---|---|---|---|
T7 | 188-191 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
T8 | 220-223 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
T9 | 269-272 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
LitCoin-GeneOrGeneProduct-v3
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T5 | 32-36 | GeneOrGeneProduct | denotes | PON1 |
LitCoin_Mondo_095
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T6 | 188-191 | DiseaseOrPhenotypicFeature | denotes | CHD | 0005010 |
T7 | 220-223 | DiseaseOrPhenotypicFeature | denotes | CHD | 0005010 |
T8 | 269-272 | DiseaseOrPhenotypicFeature | denotes | CHD | 0005010 |
LitCoin-MeSH-Disease-2
Id | Subject | Object | Predicate | Lexical cue | ID: |
---|---|---|---|---|---|
T7 | 188-191 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
T8 | 220-223 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
T9 | 269-272 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
LitCoin-MONDO_bioort2019
Id | Subject | Object | Predicate | Lexical cue | #label |
---|---|---|---|---|---|
T6 | 188-191 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
T7 | 220-223 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
T8 | 269-272 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 |
LitCoin-NCBITaxon-2
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T3 | 98-103 | OrganismTaxon | denotes | women |
LitCoin-Chemical-MeSH-CHEBI
Id | Subject | Object | Predicate | Lexical cue | ID: |
---|---|---|---|---|---|
T5 | 32-36 | ChemicalEntity | denotes | PON1 | D043303 |
LitCoin-training-merged
Id | Subject | Object | Predicate | Lexical cue | #label | ID: |
---|---|---|---|---|---|---|
T5 | 32-36 | ChemicalEntity | denotes | PON1 | D043303 | |
T57557 | 32-36 | GeneOrGeneProduct | denotes | PON1 | ||
T8 | 269-272 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 | |
T7 | 220-223 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 | |
T6 | 188-191 | DiseaseOrPhenotypicFeature | denotes | CHD | D003327 | |
T36026 | 98-103 | OrganismTaxon | denotes | women | ||
T13030 | 37-42 | SequenceVariant | denotes | 192RR |
DisGeNET5_gene_disease
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
15241482-9#32#36#gene5444 | 32-36 | gene5444 | denotes | PON1 |
15241482-9#188#191#diseaseC0010068 | 188-191 | diseaseC0010068 | denotes | CHD |
15241482-9#220#223#diseaseC0010068 | 220-223 | diseaseC0010068 | denotes | CHD |
15241482-9#269#272#diseaseC0010068 | 269-272 | diseaseC0010068 | denotes | CHD |
32#36#gene5444188#191#diseaseC0010068 | 15241482-9#32#36#gene5444 | 15241482-9#188#191#diseaseC0010068 | associated_with | PON1,CHD |
32#36#gene5444220#223#diseaseC0010068 | 15241482-9#32#36#gene5444 | 15241482-9#220#223#diseaseC0010068 | associated_with | PON1,CHD |
32#36#gene5444269#272#diseaseC0010068 | 15241482-9#32#36#gene5444 | 15241482-9#269#272#diseaseC0010068 | associated_with | PON1,CHD |