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PubMed:15064320 / 0-114 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
620 39-45 GeneOrGeneProduct denotes SRD5A2 NCBIGene:6716
621 63-87 DiseaseOrPhenotypicFeature denotes male pseudohermaphrodite MESH:D058490
622 88-95 OrganismTaxon denotes patient NCBITaxon:9606

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-114 Sentence denotes Compound heterozygous mutations in the SRD5A2 gene exon 4 in a male pseudohermaphrodite patient of Chinese origin.

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 68-87 DiseaseOrPhenotypicFeature denotes pseudohermaphrodite 0005518

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 22-31 GeneOrGeneProduct denotes mutations
T2 39-45 GeneOrGeneProduct denotes SRD5A2
T3 58-62 GeneOrGeneProduct denotes in a
T4 63-67 GeneOrGeneProduct denotes male

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 39-45 GeneOrGeneProduct denotes SRD5A2

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 63-87 DiseaseOrPhenotypicFeature denotes male pseudohermaphrodite D058490

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 39-45 GeneOrGeneProduct denotes SRD5A2

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 88-95 OrganismTaxon denotes patient

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 63-87 DiseaseOrPhenotypicFeature denotes male pseudohermaphrodite D058490

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 63-87 DiseaseOrPhenotypicFeature denotes male pseudohermaphrodite D058490

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T91472 39-45 GeneOrGeneProduct denotes SRD5A2
T95826 63-87 DiseaseOrPhenotypicFeature denotes male pseudohermaphrodite D058490
T76088 88-95 OrganismTaxon denotes patient