PMC:1183529 / 11166-12512 5 Projects
Annnotations
Below, discontinuous spans are shown in the chain model. You can change it to the bag model.
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T5293 | 22-23 | CHEBI_SO_EXT:base | denotes | b |
| T5294 | 63-66 | CHEBI_SO_EXT:DNA | denotes | DNA |
| T5295 | 67-75 | SO_EXT:biological_sequence | denotes | sequence |
| T5296 | 101-116 | SO_EXT:0000996 | denotes | predicted genes |
| T5297 | 132-137 | SO_EXT:0000704 | denotes | genes |
| T5298 | 149-153 | PR_EXT:000017653 | denotes | Fog2 |
| T5299 | 164-173 | SO_EXT:sequence_alteration_entity_or_process | denotes | mutations |
| T5300 | 177-181 | PR_EXT:000017653 | denotes | Fog2 |
| T5301 | 187-194 | UBERON:0000948 | denotes | cardiac |
| T5302 | 252-258 | SO_EXT:sequence_altered_entity_or_alteration_process | denotes | mutant |
| T5303 | 259-263 | NCBITaxon:10088 | denotes | mice |
| T5304 | 275-297 | UBERON:0002087 | denotes | atrioventricular canal |
| T5305 | 315-325 | UBERON:0002349 | denotes | myocardium |
| T5306 | 338-346 | UBERON:0005985 | denotes | coronary |
| T5307 | 347-358 | UBERON:0002049 | denotes | vasculature |
| T5308 | 365-367 | GO_EXT:reverse_transcription_or_reverse_transcriptase | denotes | RT |
| T5309 | 413-417 | PR_EXT:000017653 | denotes | Fog2 |
| T5310 | 434-445 | SO_EXT:0000673 | denotes | transcripts |
| T5311 | 457-463 | SO_EXT:sequence_altered_entity | denotes | mutant |
| T5312 | 476-485 | SO_EXT:wild_type_entity_or_quality | denotes | wild-type |
| T5313 | 486-493 | UBERON:0000922 | denotes | embryos |
| T5314 | 525-531 | SO_EXT:sequence_altered_entity_or_alteration_process | denotes | mutant |
| T5315 | 532-542 | SO_EXT:0000673 | denotes | transcript |
| T5316 | 554-568 | SO_EXT:point_mutation_entity_or_process | denotes | point mutation |
| T5317 | 575-582 | CHEBI_EXT:thymine_nucleobase_or_nucleoside_or_nucleotide_molecular_entity_or_group | denotes | thymine |
| T5318 | 586-594 | CHEBI_EXT:cytosine_nucleobase_or_nucleoside_or_nucleotide_molecular_entity_or_group | denotes | cytosine |
| T5319 | 598-600 | SO_EXT:0000028 | denotes | bp |
| T5320 | 637-643 | GO:0008380 | denotes | splice |
| T5321 | 637-654 | SO_EXT:splice_donor | denotes | splice donor site |
| T5322 | 679-683 | SO_EXT:0000147 | denotes | exon |
| T5323 | 690-698 | SO_EXT:sequence_alteration_entity_or_process | denotes | mutation |
| T5324 | 708-716 | GO:0008380 | denotes | splicing |
| T5325 | 744-753 | SO_EXT:sequence_insertion_entity_or_process | denotes | insertion |
| T5326 | 760-762 | SO_EXT:0000028 | denotes | bp |
| T5327 | 766-774 | SO_EXT:0000188 | denotes | intronic |
| T5328 | 775-783 | SO_EXT:biological_sequence | denotes | sequence |
| T5329 | 793-799 | SO_EXT:sequence_altered_entity_or_alteration_process | denotes | mutant |
| T5330 | 800-810 | SO_EXT:0000673 | denotes | transcript |
| T5331 | 829-839 | SO_EXT:0000319 | denotes | stop codon |
| T5332 | 866-875 | SO_EXT:sequence_truncation_process | denotes | truncated |
| T5333 | 876-883 | CHEBI_PR_EXT:protein | denotes | protein |
| T5334 | 922-928 | SO_EXT:sequence_altered_entity_or_alteration_process | denotes | mutant |
| T5335 | 929-933 | NCBITaxon:10088 | denotes | mice |
| T5336 | 954-958 | PR_EXT:000017653 | denotes | Fog2 |
| T5337 | 959-960 | SO_EXT:normal_or_wild_type_or_present | denotes | + |
| T5338 | 961-962 | SO_EXT:sequence_nullness_or_absence | denotes | − |
| T5339 | 964-968 | SO_EXT:sequence_nullness | denotes | null |
| T5340 | 969-975 | SO_EXT:0001023 | denotes | allele |
| T5341 | 977-983 | SO_EXT:sequence_altered_entity | denotes | mutant |
| T5342 | 997-1001 | SO_EXT:0000704 | denotes | gene |
| T5343 | 1038-1042 | NCBITaxon:10088 | denotes | mice |
| T5344 | 1050-1059 | UBERON:0000922 | denotes | embryonic |
| T5345 | 1060-1066 | GO_EXT:fatality_or_lethality | denotes | lethal |
| T5346 | 1126-1134 | SO_EXT:sequence_alteration_entity_or_process | denotes | mutation |
| T5347 | 1138-1142 | PR_EXT:000017653 | denotes | Fog2 |
| T5348 | 1174-1178 | NCBITaxon:10088 | denotes | mice |
| T5349 | 1211-1215 | PR_EXT:000017653 | denotes | Fog2 |
| T5350 | 1216-1220 | SO_EXT:sequence_nullness | denotes | null |
| T5351 | 1221-1227 | SO_EXT:sequence_altered_entity | denotes | mutant |
| T5352 | 1286-1296 | SO_EXT:0000673 | denotes | transcript |
| T5353 | 1325-1331 | GO:0008380 | denotes | splice |
| T5354 | 1325-1336 | SO_EXT:0000162 | denotes | splice site |
| T5355 | 1337-1345 | SO_EXT:sequence_alteration_entity_or_process | denotes | mutation |