Social Rewarding: Amount of References of Revisions (unweighted, directly from DB)

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Showing below up to 50 results starting with #35,701.

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  1. [R128793] Homo sapiens:Cardiomyocyte signaling converging on titin (0.00 points)
  2. [R128794] Homo sapiens:Cardiomyocyte signaling converging on titin (0.00 points)
  3. [R129750] Homo sapiens:Cardiomyocyte signaling converging on titin (0.00 points)
  4. [R140060] Homo sapiens:Cardiomyocyte signaling converging on titin (0.00 points)
  5. [R125932] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  6. [R125933] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  7. [R125934] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  8. [R125950] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  9. [R125999] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  10. [R126001] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  11. [R126004] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  12. [R126020] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  13. [R126021] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  14. [R126043] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  15. [R126044] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  16. [R126082] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  17. [R126097] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  18. [R126111] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  19. [R126161] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  20. [R126450] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  21. [R126451] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  22. [R126462] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  23. [R126541] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  24. [R126542] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  25. [R126967] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  26. [R127005] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  27. [R127025] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  28. [R127026] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  29. [R127117] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  30. [R134399] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  31. [R134458] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  32. [R134459] Homo sapiens:1p36 copy number variation syndrome (0.00 points)
  33. [R125936] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  34. [R125937] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  35. [R125998] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  36. [R126000] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  37. [R126042] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  38. [R126452] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  39. [R126453] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  40. [R127103] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  41. [R127104] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  42. [R127105] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  43. [R127106] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  44. [R127107] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  45. [R127108] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  46. [R127109] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  47. [R127110] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  48. [R134456] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  49. [R134457] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)
  50. [R139550] Homo sapiens:8p23.1 copy number variation syndrome (0.00 points)

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