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PubMed:19370764 / 453-619 JSONTXT

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PubTator4TogoVar

Id Subject Object Predicate Lexical cue proteinmutation
19370764_0 25-32 ProteinMutation denotes p.T286M rs193302860

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T4 0-166 Sentence denotes These included missense (p.T286M) and nonsense (p.W111X) mutations and a transition in the obligate AG-dinucleotide of the intron 8 acceptor splice site (c.610-2A>G).

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
5998 25-32 SequenceVariant denotes p.T286M DBSNP:rs193302860
5999 48-55 SequenceVariant denotes p.W111X DBSNP:rs137852884
6000 100-115 SequenceVariant denotes AG-dinucleotide DBSNP:rs193302855
6001 154-164 SequenceVariant denotes c.610-2A>G DBSNP:rs193302855

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T1 25-32 SequenceVariant denotes p.T286M
T2 48-55 SequenceVariant denotes p.W111X
T3 154-164 SequenceVariant denotes c.610-2A>G

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T14 15-23 GeneOrGeneProduct denotes missense
T15 57-66 GeneOrGeneProduct denotes mutations
T16 141-147 GeneOrGeneProduct denotes splice

LitCoin-training-merged

Id Subject Object Predicate Lexical cue
T32283 154-164 SequenceVariant denotes c.610-2A>G
T52346 48-55 SequenceVariant denotes p.W111X
T47349 25-32 SequenceVariant denotes p.T286M

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 25-32 ProteinMutation:p|SUB|T|286|M denotes p.T286M
T2 48-55 ProteinMutation:p|SUB|W|111|X denotes p.W111X
T3 154-164 DNAMutation:c|SUB|A|610-2|G denotes c.610-2A>G