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- NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_assertion type Assertion NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_head.
- NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_provenance.
- NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_assertion evidence source_evidence_literature NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_provenance.
- NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_assertion SIO_000772 9603439 NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_provenance.
- NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_assertion wasDerivedFrom befree-20140225 NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_provenance.
- NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_assertion wasGeneratedBy ECO_0000203 NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_provenance.