PubMed:17033686 / 1419-1659 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T10 0-240 Sentence denotes In summary, our findings demonstrate for the first time that mutations in PQBP1 are associated with an S-XLMR phenotype including microphthalmia, thereby further extending the clinical spectrum of phenotypes associated with PQBP1 mutations.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
3472 74-79 GeneOrGeneProduct denotes PQBP1 NCBIGene:10084
3473 105-109 DiseaseOrPhenotypicFeature denotes XLMR MESH:D038901
3474 130-144 DiseaseOrPhenotypicFeature denotes microphthalmia MESH:D008850
3475 224-229 GeneOrGeneProduct denotes PQBP1 NCBIGene:10084

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T12 130-144 DiseaseOrPhenotypicFeature denotes microphthalmia 0021129

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T38 16-24 GeneOrGeneProduct denotes findings
T39 51-55 GeneOrGeneProduct denotes time
T40 56-70 GeneOrGeneProduct denotes that mutations
T41 74-79 GeneOrGeneProduct denotes PQBP1
T42 105-109 GeneOrGeneProduct denotes XLMR
T43 130-144 GeneOrGeneProduct denotes microphthalmia
T44 162-171 GeneOrGeneProduct denotes extending
T45 224-229 GeneOrGeneProduct denotes PQBP1
T46 230-239 GeneOrGeneProduct denotes mutations

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T21 74-79 GeneOrGeneProduct denotes PQBP1
T22 105-109 GeneOrGeneProduct denotes XLMR
T23 130-144 GeneOrGeneProduct denotes microphthalmia
T24 224-229 GeneOrGeneProduct denotes PQBP1

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T17 130-144 DiseaseOrPhenotypicFeature denotes microphthalmia D008850

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T8 74-79 GeneOrGeneProduct denotes PQBP1
T9 224-229 GeneOrGeneProduct denotes PQBP1

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T17 130-144 DiseaseOrPhenotypicFeature denotes microphthalmia 0021129

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T21 105-109 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T22 130-144 DiseaseOrPhenotypicFeature denotes microphthalmia D008850

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T19 105-109 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T20 130-144 DiseaseOrPhenotypicFeature denotes microphthalmia D008850

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T9 224-229 GeneOrGeneProduct denotes PQBP1
T8 74-79 GeneOrGeneProduct denotes PQBP1
T20 130-144 DiseaseOrPhenotypicFeature denotes microphthalmia D008850
T19 105-109 DiseaseOrPhenotypicFeature denotes XLMR DISEASE

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T10 0-240 Sentence denotes In summary, our findings demonstrate for the first time that mutations in PQBP1 are associated with an S-XLMR phenotype including microphthalmia, thereby further extending the clinical spectrum of phenotypes associated with PQBP1 mutations.
T10 0-240 Sentence denotes In summary, our findings demonstrate for the first time that mutations in PQBP1 are associated with an S-XLMR phenotype including microphthalmia, thereby further extending the clinical spectrum of phenotypes associated with PQBP1 mutations.

DisGeNET

Id Subject Object Predicate Lexical cue
T8 74-79 gene:10084 denotes PQBP1
T9 130-144 disease:C0026010 denotes microphthalmia
T10 224-229 gene:10084 denotes PQBP1
T11 130-144 disease:C0026010 denotes microphthalmia
R5 T8 T9 associated_with PQBP1,microphthalmia
R6 T10 T11 associated_with PQBP1,microphthalmia

PubmedHPO

Id Subject Object Predicate Lexical cue
T14 130-144 HP_0000568 denotes microphthalmia

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB7 130-144 HP:0000568 denotes microphthalmia