Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_provenance.
- 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.
- uniprot-20150221 importedOn "2015-02-21" NP449.RApL60_UjS7i5n-ThYQcG6c0zfrNKT2hkeZ1LIq97urh8130_provenance.