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PubMed:16158428 / 415-658 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T4 0-243 Sentence denotes We report here a new family with X-linked mental retardation due to mutation in OPHN1 and present unpublished data about two families previously reported, concerning the facial and psychological phenotype of affected males and carrier females.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
2297 33-60 DiseaseOrPhenotypicFeature denotes X-linked mental retardation MESH:D038901
2298 80-85 GeneOrGeneProduct denotes OPHN1 NCBIGene:4983

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T10 33-41 GeneOrGeneProduct denotes X-linked
T11 65-76 GeneOrGeneProduct denotes to mutation
T12 80-85 GeneOrGeneProduct denotes OPHN1
T13 217-222 GeneOrGeneProduct denotes males
T14 227-234 GeneOrGeneProduct denotes carrier

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T4 33-41 GeneOrGeneProduct denotes X-linked
T5 80-85 GeneOrGeneProduct denotes OPHN1
T6 227-234 GeneOrGeneProduct denotes carrier

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T4 33-60 DiseaseOrPhenotypicFeature denotes X-linked mental retardation D038901

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T4 80-85 GeneOrGeneProduct denotes OPHN1

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T3 42-60 DiseaseOrPhenotypicFeature denotes mental retardation 0001071

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T3 33-60 DiseaseOrPhenotypicFeature denotes X-linked mental retardation D038901

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T3 33-60 DiseaseOrPhenotypicFeature denotes X-linked mental retardation D038901

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T4 80-85 GeneOrGeneProduct denotes OPHN1
T5680 33-60 DiseaseOrPhenotypicFeature denotes X-linked mental retardation D038901

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
16158428-3#80#85#gene4983 80-85 gene4983 denotes OPHN1
16158428-3#33#60#diseaseC1136249 33-60 diseaseC1136249 denotes X-linked mental retardation
80#85#gene498333#60#diseaseC1136249 16158428-3#80#85#gene4983 16158428-3#33#60#diseaseC1136249 associated_with OPHN1,X-linked mental retardation

DisGeNET

Id Subject Object Predicate Lexical cue
T2 80-85 gene:4983 denotes OPHN1
T3 33-60 disease:C1136249 denotes X-linked mental retardation
R2 T2 T3 associated_with OPHN1,X-linked mental retardation