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PubMed:16322221 / 182-470 JSONTXT

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c_corpus

Id Subject Object Predicate Lexical cue
T31 21-28 SO:0000104 denotes protein
T30 21-28 PR:000000001 denotes protein
T27 21-28 GO:0003675 denotes protein
T28 21-28 CHEBI:36080 denotes protein
T29 21-28 CHEBI:11122 denotes protein
T32 73-87 SO:0000289 denotes microsatellite
T33 73-99 D053842 denotes microsatellite instability
T34 73-99 D053842 denotes microsatellite instability
T35 122-127 PR:P40692 denotes hMLH1
T36 128-132 SO:0000704 denotes gene
T37 166-202 D003123 denotes hereditary nonpolyposis colon cancer
T38 166-202 D003123 denotes hereditary nonpolyposis colon cancer
T39 190-195 UBERON:0001155 denotes colon
T43 221-226 PR:P54278 denotes hPMS2

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 190-202 HP_0003003 denotes colon cancer
T2 190-202 HP_0100273 denotes colon cancer
T3 196-202 HP_0002664 denotes cancer

UseCases_ArguminSci_Discourse

Id Subject Object Predicate Lexical cue
T3 0-288 DRI_Outcome denotes Cells lacking either protein have a strong mutator phenotype and display microsatellite instability, yet mutations in the hMLH1 gene account for approximately 50% of hereditary nonpolyposis colon cancer families, whereas hPMS2 mutations are substantially less frequent and less penetrant.