PubMed:17910065 / 185-293
Annnotations
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 4417 | 3-9 | OrganismTaxon | denotes | humans | NCBITaxon:9606 |
| 4418 | 55-93 | DiseaseOrPhenotypicFeature | denotes | nonsyndromic and syndromic oligodontia | MESH:C538049 |
LitCoin-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3 | 0-108 | Sentence | denotes | In humans, mutations in both genes are associated with nonsyndromic and syndromic oligodontia, respectively. |
LitCoin-entities-OrganismTaxon-PD
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T2 | 3-9 | OrganismTaxon | denotes | humans | NCBItxid:9605 |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T10 | 11-20 | GeneOrGeneProduct | denotes | mutations |
| T11 | 72-81 | GeneOrGeneProduct | denotes | syndromic |
LitCoin-Disease-MeSH
| Id | Subject | Object | Predicate | Lexical cue | originalLabel |
|---|---|---|---|---|---|
| T1 | 72-81 | DiseaseOrPhenotypicFeature | denotes | syndromic | D013577 |
LitCoin_Mondo_095
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T2 | 82-93 | DiseaseOrPhenotypicFeature | denotes | oligodontia | 0005486 |
LitCoin-MeSH-Disease-2
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T2 | 82-93 | DiseaseOrPhenotypicFeature | denotes | oligodontia | DISEASE |
LitCoin-MONDO_bioort2019
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T2 | 82-93 | DiseaseOrPhenotypicFeature | denotes | oligodontia | DISEASE |
LitCoin-NCBITaxon-2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 3-9 | OrganismTaxon | denotes | humans |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T78294 | 82-93 | DiseaseOrPhenotypicFeature | denotes | oligodontia | DISEASE |
| T12058 | 3-9 | OrganismTaxon | denotes | humans |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T3 | 0-108 | Sentence | denotes | In humans, mutations in both genes are associated with nonsyndromic and syndromic oligodontia, respectively. |
| T3 | 0-108 | Sentence | denotes | In humans, mutations in both genes are associated with nonsyndromic and syndromic oligodontia, respectively. |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 82-93 | HP_0000677 | denotes | oligodontia |
| T1 | 82-93 | HP_0000677 | denotes | oligodontia |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 82-93 | HP:0000677 | denotes | oligodontia |
PubCasesORDO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 82-93 | ORDO:99798 | denotes | oligodontia |