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PubMed:9774399 / 0-234 JSONTXT

Annnotations TAB JSON ListView MergeView

DisGeNET

Id Subject Object Predicate Lexical cue
T0 133-138 gene:1666 denotes NADPH
T1 203-232 disease:C0018203 denotes chronic granulomatous disease
R1 T0 T1 associated_with NADPH,chronic granulomatous disease

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9774399-1#10#15#gene1666 133-138 gene1666 denotes NADPH
9774399-1#80#109#diseaseC0018203 203-232 diseaseC0018203 denotes chronic granulomatous disease
10#15#gene166680#109#diseaseC0018203 9774399-1#10#15#gene1666 9774399-1#80#109#diseaseC0018203 associated_with NADPH,chronic granulomatous disease

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-122 Sentence denotes Mutation at histidine 338 of gp91(phox) depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase.
T1 0-122 Sentence denotes Mutation at histidine 338 of gp91(phox) depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase.

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 203-232 ORDO:379 denotes chronic granulomatous disease

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 203-232 Disease denotes chronic granulomatous disease http://purl.obolibrary.org/obo/MONDO_0018305

NCBITAXON

Id Subject Object Predicate Lexical cue db_id
T1 102-107 OrganismTaxon denotes human 9606