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- NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_assertion type Assertion NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_head.
- NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_assertion description "[For example, mutations in CLN5, CLN6, MFSD8, or CLN8 can underlie the clinically similar late infantile variant NCL disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_provenance.
- NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_assertion evidence source_evidence_curated NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_provenance.
- NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_assertion SIO_000772 21990111 NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_provenance.
- NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_assertion wasDerivedFrom uniprot-20150221 NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_provenance.
- NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_assertion wasGeneratedBy ECO_0000218 NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_provenance.