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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking NBN and hereditary breast ovarian cancer syndrome in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 168 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 0 papers in RGD have been used to annotate NBN
  • Curation Notes: ClinVar Annotator: match by term: Breast and/or ovarian cancer | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 1 | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 2 | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:10398434 PMID:10799436 PMID:10848790 PMID:10852373 PMID:11093281 PMID:11279524 PMID:11325820 PMID:11953735 PMID:12123493 PMID:12353271 PMID:12505263 PMID:12833396 PMID:12845677 PMID:14559852 PMID:14973119 PMID:15185344 PMID:15279809 PMID:15338273 PMID:16033915 PMID:16199547 PMID:16415040 PMID:16474176 PMID:16544999 PMID:16810201 PMID:17001621 PMID:17103455 PMID:17576681 PMID:17695489 PMID:17894553 PMID:17899368 PMID:18023021 PMID:18049891 PMID:18280732 PMID:18281469 PMID:18606567 PMID:18612309 PMID:18638378 PMID:18940477 PMID:19393249 PMID:19452044 PMID:19523210 PMID:19584272 PMID:19635536 PMID:19813148 PMID:19908051 PMID:20444919 PMID:21212067 PMID:21302341 PMID:21698754 PMID:22131123 PMID:22293976 PMID:22373003 PMID:22491912 PMID:22841127 PMID:22864661 PMID:22941933 PMID:22995991 PMID:23317186 PMID:23555315 PMID:24033266 PMID:24093751 PMID:24113799 PMID:24349281 PMID:24549055 PMID:24728327 PMID:24830725 PMID:25117502 PMID:25186627 PMID:25318351 PMID:25485873 PMID:25503501 PMID:25619955 PMID:25712764 PMID:25741868 PMID:25980754 PMID:26083025 PMID:26315354 PMID:26467025 PMID:26580448 PMID:26722329 PMID:26787654 PMID:26822949 PMID:26845104 PMID:26898890 PMID:26976419 PMID:27150568 PMID:27153395 PMID:27443514 PMID:27616075 PMID:27621404 PMID:27978560 PMID:28076423 PMID:28135145 PMID:28261280 PMID:28376765 PMID:28492532 PMID:28528518 PMID:28591191 PMID:28873162 PMID:29335925 PMID:29368341 PMID:29419426 PMID:29522266 PMID:29625052 PMID:29678143 PMID:29785153 PMID:30287823 PMID:30306255 PMID:30426508 PMID:30441849 PMID:30564542 PMID:30590007 PMID:30651582 PMID:30942098 PMID:30982232 PMID:31159747 PMID:31173646 PMID:31415627 PMID:31666926 PMID:32068069 PMID:32295079 PMID:32566746 PMID:32906206 PMID:32980694 PMID:33050356 PMID:33309985 PMID:33471974 PMID:33471991 PMID:33800431 PMID:33840814 PMID:34072463 PMID:34072659 PMID:34544220 PMID:35309086 PMID:9536098 PMID:9590180 PMID:9590181 PMID:9620777


  • An association has been curated linking NBN and hereditary breast ovarian cancer syndrome in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 168 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 0 papers in RGD have been used to annotate NBN
  • Curation Notes: ClinVar Annotator: match by term: Breast and/or ovarian cancer | ClinVar Annotator: match by term: Breast-ovarian cancer, familial 2 | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 1 | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 2 | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 3 | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 4 | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:10398434 PMID:10852373 PMID:11093281 PMID:11279524 PMID:11325820 PMID:11953735 PMID:12123493 PMID:12353271 PMID:12505263 PMID:12833396 PMID:14559852 PMID:14973119 PMID:15185344 PMID:15338273 PMID:16033915 PMID:16199547 PMID:16415040 PMID:16474176 PMID:16544999 PMID:16810201 PMID:17001621 PMID:17103455 PMID:17576681 PMID:17695489 PMID:17894553 PMID:17899368 PMID:18023021 PMID:18049891 PMID:18280732 PMID:18281469 PMID:18606567 PMID:18612309 PMID:18638378 PMID:18940477 PMID:19393249 PMID:19452044 PMID:19523210 PMID:19584272 PMID:19635536 PMID:19813148 PMID:19908051 PMID:20444919 PMID:21212067 PMID:21302341 PMID:21698754 PMID:22131123 PMID:22293976 PMID:22373003 PMID:22841127 PMID:22864661 PMID:22941933 PMID:22995991 PMID:23317186 PMID:23555315 PMID:23765759 PMID:24033266 PMID:24093751 PMID:24113799 PMID:24349281 PMID:24549055 PMID:24728327 PMID:24830725 PMID:25117502 PMID:25186627 PMID:25318351 PMID:25485873 PMID:25503501 PMID:25619955 PMID:25712764 PMID:25741868 PMID:25980754 PMID:26083025 PMID:26315354 PMID:26467025 PMID:26580448 PMID:26681312 PMID:26722329 PMID:26787654 PMID:26822949 PMID:26845104 PMID:26898890 PMID:26976419 PMID:27150568 PMID:27153395 PMID:27443514 PMID:27616075 PMID:27621404 PMID:27978560 PMID:28076423 PMID:28135145 PMID:28261280 PMID:28376765 PMID:28492532 PMID:28528518 PMID:28591191 PMID:28873162 PMID:29335925 PMID:29368341 PMID:29522266 PMID:29625052 PMID:29678143 PMID:29785153 PMID:30287823 PMID:30426508 PMID:30441849 PMID:30564542 PMID:30590007 PMID:30651582 PMID:30942098 PMID:30982232 PMID:31159747 PMID:31173646 PMID:31415627 PMID:31666926 PMID:32068069 PMID:32295079 PMID:32566746 PMID:32906206 PMID:32980694 PMID:33309985 PMID:33800431 PMID:9536098 PMID:9590180 PMID:9620777


  • An association has been curated linking NBN and hereditary breast ovarian cancer syndrome in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 168 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 0 papers in RGD have been used to annotate NBN
  • Curation Notes: ClinVar Annotator: match by term: Breast and/or ovarian cancer | ClinVar Annotator: match by term: Breast-ovarian cancer, familial 1 | ClinVar Annotator: match by term: Breast-ovarian cancer, familial 2 | ClinVar Annotator: match by term: Hereditary breast and ovarian cancer syndrome
  • Original References(s): PMID:10398434 PMID:10852373 PMID:11093281 PMID:11279524 PMID:11325820 PMID:11953735 PMID:12123493 PMID:12505263 PMID:12833396 PMID:14559852 PMID:14973119 PMID:15185344 PMID:15338273 PMID:16033915 PMID:16199547 PMID:16415040 PMID:16474176 PMID:16544999 PMID:16810201 PMID:17103455 PMID:17576681 PMID:17695489 PMID:17894553 PMID:17899368 PMID:18049891 PMID:18280732 PMID:18606567 PMID:18940477 PMID:19393249 PMID:19452044 PMID:19523210 PMID:19635536 PMID:19813148 PMID:19908051 PMID:20444919 PMID:21212067 PMID:21698754 PMID:22131123 PMID:22293976 PMID:22373003 PMID:22941933 PMID:23317186 PMID:23555315 PMID:23765759 PMID:24033266 PMID:24093751 PMID:24113799 PMID:24349281 PMID:24549055 PMID:24728327 PMID:24830725 PMID:25186627 PMID:25485873 PMID:25503501 PMID:25619955 PMID:25712764 PMID:25741868 PMID:25980754 PMID:26083025 PMID:26315354 PMID:26467025 PMID:26681312 PMID:26722329 PMID:26822949 PMID:26845104 PMID:27150568 PMID:27153395 PMID:27616075 PMID:27621404 PMID:28076423 PMID:28261280 PMID:28376765 PMID:28492532 PMID:28591191 PMID:28873162 PMID:29335925 PMID:29522266 PMID:29678143 PMID:29785153 PMID:30287823 PMID:30441849 PMID:30590007 PMID:30651582 PMID:30942098 PMID:30982232 PMID:31159747 PMID:31173646 PMID:31666926 PMID:32068069 PMID:32295079 PMID:32566746 PMID:33309985 PMID:33800431 PMID:9536098 PMID:9590180 PMID:9620777


  • An association has been curated linking NBN and hereditary breast ovarian cancer syndrome in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 168 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 0 papers in RGD have been used to annotate NBN
  • Curation Notes: ClinVar Annotator: match by term: Breast and/or ovarian cancer | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 1 | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 2 | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:10398434 PMID:10799436 PMID:10852373 PMID:11093281 PMID:11279524 PMID:11325820 PMID:11953735 PMID:12123493 PMID:12353271 PMID:12505263 PMID:12833396 PMID:14559852 PMID:14973119 PMID:15185344 PMID:15338273 PMID:16033915 PMID:16199547 PMID:16415040 PMID:16474176 PMID:16544999 PMID:16810201 PMID:17001621 PMID:17103455 PMID:17576681 PMID:17695489 PMID:17894553 PMID:17899368 PMID:18023021 PMID:18049891 PMID:18280732 PMID:18281469 PMID:18606567 PMID:18612309 PMID:18638378 PMID:18940477 PMID:19393249 PMID:19452044 PMID:19523210 PMID:19584272 PMID:19635536 PMID:19813148 PMID:19908051 PMID:20444919 PMID:21212067 PMID:21302341 PMID:21698754 PMID:22131123 PMID:22293976 PMID:22373003 PMID:22841127 PMID:22864661 PMID:22941933 PMID:22995991 PMID:23317186 PMID:23555315 PMID:24033266 PMID:24093751 PMID:24113799 PMID:24349281 PMID:24549055 PMID:24728327 PMID:24830725 PMID:25117502 PMID:25186627 PMID:25318351 PMID:25503501 PMID:25619955 PMID:25712764 PMID:25741868 PMID:25980754 PMID:26083025 PMID:26315354 PMID:26467025 PMID:26580448 PMID:26722329 PMID:26787654 PMID:26822949 PMID:26845104 PMID:26898890 PMID:26976419 PMID:27150568 PMID:27153395 PMID:27443514 PMID:27616075 PMID:27621404 PMID:27978560 PMID:28076423 PMID:28135145 PMID:28261280 PMID:28376765 PMID:28492532 PMID:28528518 PMID:28591191 PMID:28873162 PMID:29335925 PMID:29368341 PMID:29522266 PMID:29625052 PMID:29678143 PMID:29785153 PMID:30287823 PMID:30426508 PMID:30441849 PMID:30564542 PMID:30590007 PMID:30651582 PMID:30942098 PMID:30982232 PMID:31159747 PMID:31415627 PMID:31666926 PMID:32068069 PMID:32295079 PMID:32566746 PMID:32906206 PMID:32980694 PMID:33309985 PMID:33471991 PMID:33800431 PMID:34072463 PMID:9536098 PMID:9590180 PMID:9620777


  • An association has been curated linking NBN and hereditary breast ovarian cancer syndrome in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 168 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 0 papers in RGD have been used to annotate NBN
  • Curation Notes: ClinVar Annotator: match by term: Breast and/or ovarian cancer | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 1 | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 2 | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 4 | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:10398434 PMID:10799436 PMID:10848790 PMID:10852373 PMID:11093281 PMID:11279524 PMID:11325820 PMID:11953735 PMID:12123493 PMID:12353271 PMID:12505263 PMID:12833396 PMID:12845677 PMID:14559852 PMID:14973119 PMID:15185344 PMID:15279809 PMID:15338273 PMID:16033915 PMID:16199547 PMID:16415040 PMID:16474176 PMID:16544999 PMID:16810201 PMID:17001621 PMID:17103455 PMID:17576681 PMID:17695489 PMID:17894553 PMID:17899368 PMID:18023021 PMID:18049891 PMID:18280732 PMID:18281469 PMID:18606567 PMID:18612309 PMID:18638378 PMID:18940477 PMID:19393249 PMID:19452044 PMID:19523210 PMID:19584272 PMID:19635536 PMID:19813148 PMID:19908051 PMID:20444919 PMID:21212067 PMID:21302341 PMID:21698754 PMID:22131123 PMID:22293976 PMID:22373003 PMID:22491912 PMID:22841127 PMID:22864661 PMID:22941933 PMID:22995991 PMID:23317186 PMID:23555315 PMID:24033266 PMID:24093751 PMID:24113799 PMID:24349281 PMID:24549055 PMID:24728327 PMID:24830725 PMID:25117502 PMID:25186627 PMID:25318351 PMID:25326637 PMID:25485873 PMID:25503501 PMID:25619955 PMID:25712764 PMID:25741868 PMID:25980754 PMID:26083025 PMID:26315354 PMID:26467025 PMID:26580448 PMID:26722329 PMID:26787654 PMID:26822949 PMID:26845104 PMID:26898890 PMID:26976419 PMID:27150568 PMID:27153395 PMID:27443514 PMID:27616075 PMID:27621404 PMID:27978560 PMID:28076423 PMID:28135145 PMID:28261280 PMID:28376765 PMID:28492532 PMID:28528518 PMID:28591191 PMID:28873162 PMID:29335925 PMID:29368341 PMID:29419426 PMID:29522266 PMID:29625052 PMID:29678143 PMID:29785153 PMID:30287823 PMID:30306255 PMID:30426508 PMID:30441849 PMID:30564542 PMID:30590007 PMID:30651582 PMID:30942098 PMID:30982232 PMID:31159747 PMID:31173646 PMID:31415627 PMID:31666926 PMID:32068069 PMID:32295079 PMID:32566746 PMID:32906206 PMID:32980694 PMID:33050356 PMID:33309985 PMID:33471974 PMID:33471991 PMID:33800431 PMID:33840814 PMID:34072463 PMID:34072659 PMID:34544220 PMID:35309086 PMID:9536098 PMID:9590180 PMID:9590181 PMID:9620777


  • An association has been curated linking NBN and hereditary breast ovarian cancer syndrome in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 168 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 0 papers in RGD have been used to annotate NBN
  • Curation Notes: ClinVar Annotator: match by term: Breast and/or ovarian cancer | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 1 | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 2 | ClinVar Annotator: match by term: Hereditary breast and ovarian cancer | ClinVar Annotator: match by term: Hereditary breast and ovarian cancer syndrome | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:10398434 PMID:10799436 PMID:10848790 PMID:10852373 PMID:11093281 PMID:11279524 PMID:11325820 PMID:11953735 PMID:12123493 PMID:12353271 PMID:12505263 PMID:12833396 PMID:12845677 PMID:14559852 PMID:14973119 PMID:15185344 PMID:15279809 PMID:15338273 PMID:16033915 PMID:16199547 PMID:16415040 PMID:16474176 PMID:16544999 PMID:16810201 PMID:17001621 PMID:17103455 PMID:17576681 PMID:17695489 PMID:17894553 PMID:17899368 PMID:18023021 PMID:18049891 PMID:18280732 PMID:18281469 PMID:18606567 PMID:18612309 PMID:18638378 PMID:18940477 PMID:19393249 PMID:19452044 PMID:19523210 PMID:19584272 PMID:19635536 PMID:19813148 PMID:19908051 PMID:20444919 PMID:21212067 PMID:21302341 PMID:21698754 PMID:22131123 PMID:22293976 PMID:22373003 PMID:22491912 PMID:22841127 PMID:22864661 PMID:22941933 PMID:22995991 PMID:23317186 PMID:23555315 PMID:24033266 PMID:24093751 PMID:24113799 PMID:24349281 PMID:24549055 PMID:24728327 PMID:24830725 PMID:25117502 PMID:25186627 PMID:25318351 PMID:25485873 PMID:25503501 PMID:25619955 PMID:25712764 PMID:25741868 PMID:25980754 PMID:26083025 PMID:26315354 PMID:26467025 PMID:26580448 PMID:26722329 PMID:26787654 PMID:26822949 PMID:26845104 PMID:26898890 PMID:26976419 PMID:27150568 PMID:27153395 PMID:27443514 PMID:27616075 PMID:27621404 PMID:27978560 PMID:28076423 PMID:28135145 PMID:28261280 PMID:28376765 PMID:28492532 PMID:28528518 PMID:28591191 PMID:28873162 PMID:29335925 PMID:29368341 PMID:29419426 PMID:29522266 PMID:29625052 PMID:29678143 PMID:29785153 PMID:30287823 PMID:30306255 PMID:30426508 PMID:30441849 PMID:30564542 PMID:30590007 PMID:30651582 PMID:30942098 PMID:30982232 PMID:31159747 PMID:31173646 PMID:31415627 PMID:31666926 PMID:32068069 PMID:32295079 PMID:32566746 PMID:32906206 PMID:32980694 PMID:33050356 PMID:33309985 PMID:33471974 PMID:33471991 PMID:33800431 PMID:33840814 PMID:34072463 PMID:34072659 PMID:34284872 PMID:34544220 PMID:34994648 PMID:35309086 PMID:36451132 PMID:9536098 PMID:9590180 PMID:9590181 PMID:9620777


  • An association has been curated linking NBN and hereditary breast ovarian cancer syndrome in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NBN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 168 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 0 papers in RGD have been used to annotate NBN
  • Curation Notes: ClinVar Annotator: match by term: Breast and/or ovarian cancer | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 1 | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 4 | ClinVar Annotator: match by term: Hereditary breast and ovarian cancer | ClinVar Annotator: match by term: Hereditary breast and ovarian cancer syndrome | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:10398434 PMID:10799436 PMID:10848790 PMID:10852373 PMID:11093281 PMID:11279524 PMID:11325820 PMID:11953735 PMID:12123493 PMID:12353271 PMID:12505263 PMID:12833396 PMID:12845677 PMID:14559852 PMID:14973119 PMID:15185344 PMID:15279809 PMID:15338273 PMID:16033915 PMID:16199547 PMID:16415040 PMID:16474176 PMID:16544999 PMID:16810201 PMID:17001621 PMID:17103455 PMID:17576681 PMID:17695489 PMID:17894553 PMID:17899368 PMID:18023021 PMID:18049891 PMID:18280732 PMID:18281469 PMID:18606567 PMID:18612309 PMID:18638378 PMID:18940477 PMID:19393249 PMID:19452044 PMID:19523210 PMID:19584272 PMID:19635536 PMID:19813148 PMID:19908051 PMID:20444919 PMID:21212067 PMID:21302341 PMID:21698754 PMID:22131123 PMID:22293976 PMID:22373003 PMID:22491912 PMID:22841127 PMID:22864661 PMID:22941933 PMID:22995991 PMID:23317186 PMID:23555315 PMID:24033266 PMID:24093751 PMID:24113799 PMID:24349281 PMID:24549055 PMID:24728327 PMID:24830725 PMID:25117502 PMID:25186627 PMID:25318351 PMID:25326637 PMID:25485873 PMID:25503501 PMID:25619955 PMID:25712764 PMID:25741868 PMID:25980754 PMID:26083025 PMID:26315354 PMID:26467025 PMID:26580448 PMID:26722329 PMID:26787654 PMID:26822949 PMID:26845104 PMID:26898890 PMID:26976419 PMID:27150568 PMID:27153395 PMID:27443514 PMID:27616075 PMID:27621404 PMID:27978560 PMID:28076423 PMID:28135145 PMID:28261280 PMID:28376765 PMID:28492532 PMID:28528518 PMID:28591191 PMID:28873162 PMID:29335925 PMID:29368341 PMID:29419426 PMID:29522266 PMID:29625052 PMID:29678143 PMID:29785153 PMID:30287823 PMID:30306255 PMID:30426508 PMID:30441849 PMID:30564542 PMID:30590007 PMID:30651582 PMID:30942098 PMID:30982232 PMID:31159747 PMID:31173646 PMID:31415627 PMID:31666926 PMID:32068069 PMID:32295079 PMID:32566746 PMID:32906206 PMID:32959997 PMID:32980694 PMID:33050356 PMID:33309985 PMID:33471974 PMID:33471991 PMID:33800431 PMID:33840814 PMID:34072463 PMID:34072659 PMID:34284872 PMID:34439939 PMID:34544220 PMID:34994648 PMID:35264596 PMID:35309086 PMID:36346689 PMID:36451132 PMID:9536098 PMID:9590180 PMID:9590181 PMID:9620777


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