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PubMed:21045008 / 630-755 JSONTXT

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Inflammaging

Id Subject Object Predicate Lexical cue
T8 0-125 Sentence denotes Cystic fibrosis (CF) is a multisystem disease caused by mutations in the gene encoding the CF transmembrane regulator (CFTR).
T8 0-125 Sentence denotes Cystic fibrosis (CF) is a multisystem disease caused by mutations in the gene encoding the CF transmembrane regulator (CFTR).

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T8 0-125 Sentence denotes Cystic fibrosis (CF) is a multisystem disease caused by mutations in the gene encoding the CF transmembrane regulator (CFTR).
T7 0-125 Sentence denotes Cystic fibrosis (CF) is a multisystem disease caused by mutations in the gene encoding the CF transmembrane regulator (CFTR).
T8 0-125 Sentence denotes Cystic fibrosis (CF) is a multisystem disease caused by mutations in the gene encoding the CF transmembrane regulator (CFTR).

ICD10

Id Subject Object Predicate Lexical cue
T2 0-15 http://purl.bioontology.org/ontology/ICD10/E84 denotes Cystic fibrosis
T4 0-15 http://purl.bioontology.org/ontology/ICD10/E84.9 denotes Cystic fibrosis

GlycoBiology-FMA

Id Subject Object Predicate Lexical cue
_T25 73-77 FMAID:198663 denotes gene

uniprot-human

Id Subject Object Predicate Lexical cue
T16 119-123 http://www.uniprot.org/uniprot/P13569 denotes CFTR

uniprot-mouse

Id Subject Object Predicate Lexical cue
T1 119-123 http://www.uniprot.org/uniprot/P26361 denotes CFTR

GO-BP

Id Subject Object Predicate Lexical cue
T5 108-117 http://purl.obolibrary.org/obo/GO_0065007 denotes regulator

GO-CC

Id Subject Object Predicate Lexical cue
T1 94-107 http://purl.obolibrary.org/obo/GO_0016021 denotes transmembrane
T2 94-107 http://purl.obolibrary.org/obo/GO_0044214 denotes transmembrane

Allie

Id Subject Object Predicate Lexical cue
SS1_21045008_6_0 0-15 expanded denotes Cystic fibrosis
SS2_21045008_6_0 17-19 abbr denotes CF
SS1_21045008_6_1 91-117 expanded denotes CF transmembrane regulator
SS2_21045008_6_1 119-123 abbr denotes CFTR
AE1_21045008_6_0 SS1_21045008_6_0 SS2_21045008_6_0 abbreviatedTo Cystic fibrosis,CF
AE1_21045008_6_1 SS1_21045008_6_1 SS2_21045008_6_1 abbreviatedTo CF transmembrane regulator,CFTR

EDAM-topics

Id Subject Object Predicate Lexical cue
T7 38-45 http://edamontology.org/topic_0634 denotes disease
T8 56-65 http://edamontology.org/topic_0199 denotes mutations
T9 94-117 http://edamontology.org/topic_0736 denotes transmembrane regulator

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T4 0-15 Disease denotes Cystic fibrosis http://purl.obolibrary.org/obo/MONDO_0009061
T5 17-19 Disease denotes CF http://purl.obolibrary.org/obo/MONDO_0009061
T6 91-93 Disease denotes CF http://purl.obolibrary.org/obo/MONDO_0009061

Lectin-Jamboree-Sentence

Id Subject Object Predicate Lexical cue
T7 0-125 Sentence denotes Cystic fibrosis (CF) is a multisystem disease caused by mutations in the gene encoding the CF transmembrane regulator (CFTR).

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T4 94-107 Body_part denotes transmembrane http://purl.obolibrary.org/obo/GO_0016020