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PubMed:8702490 / 191-403 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T2 0-212 Sentence denotes Achondrogenesis type 1B is an autosomal recessive, lethal chondrodysplasia caused by mutations in the gene encoding a sulfate/chloride antiporter of the cell membrane (Superti-Furga, A., Hästbacka, J., Wilcox, W.
T2 0-212 Sentence denotes Achondrogenesis type 1B is an autosomal recessive, lethal chondrodysplasia caused by mutations in the gene encoding a sulfate/chloride antiporter of the cell membrane (Superti-Furga, A., Hästbacka, J., Wilcox, W.

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T3 0-23 Disease denotes Achondrogenesis type 1B http://purl.obolibrary.org/obo/MONDO_0010966
T4 51-74 Disease denotes lethal chondrodysplasia http://purl.obolibrary.org/obo/MONDO_0019718

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T2 153-166 Body_part denotes cell membrane http://purl.obolibrary.org/obo/GO_0005886