PMC:549712 / 7903-9362 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 |
|---|---|---|---|---|
| T2573 | 44-62 | CHEBI:18303 | denotes | phosphatidylserine |
| T2574 | 44-71 | PR_EXT:000009218 | denotes | phosphatidylserine receptor |
| T2575 | 63-71 | GO_EXT:0004872 | denotes | receptor |
| T2576 | 72-77 | PR_EXT:000009218 | denotes | Ptdsr |
| T2577 | 94-98 | SO_EXT:sequence_nullness | denotes | null |
| T2578 | 99-105 | SO_EXT:0001023 | denotes | allele |
| T2579 | 113-118 | NCBITaxon:10088 | denotes | mouse |
| T2580 | 122-126 | SO_EXT:0000704 | denotes | gene |
| T2581 | 192-197 | PR_EXT:000009218 | denotes | Ptdsr |
| T2582 | 207-211 | NCBITaxon:10088 | denotes | mice |
| T2583 | 236-245 | UBERON:0000922 | denotes | embryonic |
| T2584 | 236-250 | _FRAGMENT | denotes | embryonic stem |
| T2586 | 252-254 | _FRAGMENT | denotes | ES |
| T2585 | 256-261 | CL:0002322 | denotes | cells |
| T2587 | 256-261 | CL_GO_EXT:cell | denotes | cells |
| T2588 | 266-270 | SO_EXT:0000704 | denotes | gene |
| T2589 | 305-310 | PR_EXT:000009218 | denotes | Ptdsr |
| T2590 | 311-315 | SO_EXT:sequence_nullness | denotes | null |
| T2591 | 316-322 | SO_EXT:0001023 | denotes | allele |
| T2592 | 352-359 | SO_EXT:0000704 | denotes | genetic |
| T2593 | 403-408 | NCBITaxon:10088 | denotes | mouse |
| T2594 | 424-429 | PR_EXT:000009218 | denotes | Ptdsr |
| T2595 | 462-467 | PR_EXT:000009218 | denotes | Ptdsr |
| T2596 | 468-469 | SO_EXT:sequence_nullness_or_absence | denotes | - |
| T2597 | 470-471 | SO_EXT:sequence_nullness_or_absence | denotes | - |
| T2598 | 487-492 | PR_EXT:000009218 | denotes | Ptdsr |
| T2599 | 492-493 | SO_EXT:normal_or_wild_type_or_present | denotes | + |
| T2600 | 494-495 | SO_EXT:sequence_nullness_or_absence | denotes | - |
| T2601 | 496-500 | NCBITaxon:10088 | denotes | mice |
| T2602 | 562-567 | PR_EXT:000009218 | denotes | Ptdsr |
| T2603 | 568-569 | SO_EXT:normal_or_wild_type_or_present | denotes | + |
| T2604 | 570-571 | SO_EXT:sequence_nullness_or_absence | denotes | - |
| T2605 | 572-576 | NCBITaxon:10088 | denotes | mice |
| T2606 | 618-623 | PR_EXT:000009218 | denotes | Ptdsr |
| T2607 | 634-638 | NCBITaxon:10088 | denotes | mice |
| T2608 | 655-660 | PR_EXT:000009218 | denotes | Ptdsr |
| T2609 | 661-671 | GO:0010467 | denotes | expression |
| T2610 | 675-680 | PR_EXT:000009218 | denotes | Ptdsr |
| T2611 | 681-682 | SO_EXT:sequence_nullness_or_absence | denotes | - |
| T2612 | 683-684 | SO_EXT:sequence_nullness_or_absence | denotes | - |
| T2613 | 685-692 | UBERON:0000922 | denotes | embryos |
| T2614 | 710-712 | GO_EXT:reverse_transcription_or_reverse_transcriptase | denotes | RT |
| T2615 | 801-809 | GO_EXT:breeding | denotes | breeding |
| T2616 | 826-830 | NCBITaxon:10088 | denotes | mice |
| T2617 | 847-855 | SO_EXT:sequence_alteration_entity_or_process | denotes | mutation |
| T2618 | 860-866 | GO_EXT:fatality_or_lethality | denotes | lethal |
| T2619 | 885-892 | SO_EXT:sequence_altered_entity | denotes | mutants |
| T2620 | 979-988 | UBERON:0000922 | denotes | embryonic |
| T2621 | 979-1000 | GO:0009790 | denotes | embryonic development |
| T2622 | 1017-1022 | PR_EXT:000009218 | denotes | Ptdsr |
| T2623 | 1029-1037 | SO_EXT:sequence_alteration_entity_or_process | denotes | mutation |
| T2624 | 1045-1054 | GO_EXT:breeding | denotes | breedings |
| T2625 | 1102-1109 | UBERON:0000922 | denotes | embryos |
| T2626 | 1169-1176 | UBERON:0000922 | denotes | embryos |
| T2627 | 1198-1203 | PR_EXT:000009218 | denotes | Ptdsr |
| T2628 | 1203-1204 | SO_EXT:normal_or_wild_type_or_present | denotes | + |
| T2629 | 1205-1206 | SO_EXT:sequence_nullness_or_absence | denotes | - |
| T2630 | 1206-1210 | NCBITaxon:10088 | denotes | mice |
| T2631 | 1234-1241 | UBERON:0000922 | denotes | embryos |
| T2632 | 1259-1270 | GO:0007565 | denotes | gestational |
| T2633 | 1306-1311 | PR_EXT:000009218 | denotes | Ptdsr |
| T2634 | 1333-1340 | UBERON:0000922 | denotes | embryos |
| T2635 | 1388-1396 | SO_EXT:sequence_alteration_entity_or_process | denotes | mutation |
| T2636 | 1430-1439 | UBERON:0000922 | denotes | embryonic |
| T2637 | 1440-1449 | GO_EXT:fatality_or_lethality | denotes | lethality |
| R1342 | T2585 | T2584 | _lexicallyChainedTo | cells,embryonic stem |
| R1343 | T2585 | T2586 | _lexicallyChainedTo | cells,ES |