Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_assertion> ?p ?o ?g. }
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- NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_assertion type Assertion NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_head.
- NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_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." NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_provenance.
- NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_assertion evidence source_evidence_literature NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_provenance.
- NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_assertion SIO_000772 9603439 NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_provenance.
- NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_assertion wasDerivedFrom befree-20150227 NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_provenance.
- NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_assertion wasGeneratedBy ECO_0000203 NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_provenance.