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PubMed:17033686 / 116-387 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T2 0-271 Sentence denotes X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
3450 0-27 DiseaseOrPhenotypicFeature denotes X-linked mental retardation MESH:D038901
3451 77-81 DiseaseOrPhenotypicFeature denotes XLMR MESH:D038901
3452 111-115 DiseaseOrPhenotypicFeature denotes XLMR MESH:D038901
3453 228-233 GeneOrGeneProduct denotes PQBP1 NCBIGene:10084
3454 247-251 DiseaseOrPhenotypicFeature denotes XLMR MESH:D038901
3455 266-270 DiseaseOrPhenotypicFeature denotes XLMR MESH:D038901

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T5 0-8 GeneOrGeneProduct denotes X-linked
T6 64-73 GeneOrGeneProduct denotes syndromic
T7 77-81 GeneOrGeneProduct denotes XLMR
T8 91-100 GeneOrGeneProduct denotes syndromic
T9 111-115 GeneOrGeneProduct denotes XLMR
T10 168-173 GeneOrGeneProduct denotes begin
T11 188-197 GeneOrGeneProduct denotes mutations
T12 228-233 GeneOrGeneProduct denotes PQBP1
T13 247-251 GeneOrGeneProduct denotes XLMR
T14 266-270 GeneOrGeneProduct denotes XLMR

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T3 0-8 GeneOrGeneProduct denotes X-linked
T4 77-81 GeneOrGeneProduct denotes XLMR
T5 111-115 GeneOrGeneProduct denotes XLMR
T6 228-233 GeneOrGeneProduct denotes PQBP1
T7 247-251 GeneOrGeneProduct denotes XLMR
T8 266-270 GeneOrGeneProduct denotes XLMR

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T4 0-27 DiseaseOrPhenotypicFeature denotes X-linked mental retardation D038901
T5 64-73 DiseaseOrPhenotypicFeature denotes syndromic D013577
T6 91-100 DiseaseOrPhenotypicFeature denotes syndromic D013577

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T2 228-233 GeneOrGeneProduct denotes PQBP1

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T4 9-27 DiseaseOrPhenotypicFeature denotes mental retardation 0001071
T5 108-110 DiseaseOrPhenotypicFeature denotes NS 0009735
T6 235-238 DiseaseOrPhenotypicFeature denotes can 0012833
T7 263-265 DiseaseOrPhenotypicFeature denotes NS 0009735

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T4 0-27 DiseaseOrPhenotypicFeature denotes X-linked mental retardation D038901
T5 77-81 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T6 111-115 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T7 247-251 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T8 266-270 DiseaseOrPhenotypicFeature denotes XLMR DISEASE

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T4 0-27 DiseaseOrPhenotypicFeature denotes X-linked mental retardation D038901
T5 77-81 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T6 111-115 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T7 247-251 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T8 266-270 DiseaseOrPhenotypicFeature denotes XLMR DISEASE

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T2 228-233 GeneOrGeneProduct denotes PQBP1
T44580 266-270 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T87219 247-251 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T6556 111-115 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T59750 77-81 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T30956 0-27 DiseaseOrPhenotypicFeature denotes X-linked mental retardation D038901

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T2 0-271 Sentence denotes X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR.
T2 0-271 Sentence denotes X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR.

DisGeNET

Id Subject Object Predicate Lexical cue
T0 77-81 gene:1741 denotes XLMR
T1 0-27 disease:C1136249 denotes X-linked mental retardation
T2 111-115 gene:1741 denotes XLMR
T3 0-27 disease:C1136249 denotes X-linked mental retardation
T4 247-251 gene:1741 denotes XLMR
T5 0-27 disease:C1136249 denotes X-linked mental retardation
R1 T0 T1 associated_with XLMR,X-linked mental retardation
R2 T2 T3 associated_with XLMR,X-linked mental retardation
R3 T4 T5 associated_with XLMR,X-linked mental retardation

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 0-8 HP_0001417 denotes X-linked
T2 9-27 HP_0001249 denotes mental retardation

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
17033686-1#77#81#gene1741 77-81 gene1741 denotes XLMR
17033686-1#111#115#gene1741 111-115 gene1741 denotes XLMR
17033686-1#228#233#gene10084 228-233 gene10084 denotes PQBP1
17033686-1#247#251#gene1741 247-251 gene1741 denotes XLMR
17033686-1#266#270#gene1741 266-270 gene1741 denotes XLMR
17033686-1#0#27#diseaseC1136249 0-27 diseaseC1136249 denotes X-linked mental retardation
77#81#gene17410#27#diseaseC1136249 17033686-1#77#81#gene1741 17033686-1#0#27#diseaseC1136249 associated_with XLMR,X-linked mental retardation
111#115#gene17410#27#diseaseC1136249 17033686-1#111#115#gene1741 17033686-1#0#27#diseaseC1136249 associated_with XLMR,X-linked mental retardation
228#233#gene100840#27#diseaseC1136249 17033686-1#228#233#gene10084 17033686-1#0#27#diseaseC1136249 associated_with PQBP1,X-linked mental retardation
247#251#gene17410#27#diseaseC1136249 17033686-1#247#251#gene1741 17033686-1#0#27#diseaseC1136249 associated_with XLMR,X-linked mental retardation
266#270#gene17410#27#diseaseC1136249 17033686-1#266#270#gene1741 17033686-1#0#27#diseaseC1136249 associated_with XLMR,X-linked mental retardation