Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_assertion> ?p ?o ?g. }
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- NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_assertion type Assertion NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_head.
- NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_assertion description "[The retinal degeneration in this patient is most likely to be secondary to a genetic disorder of autosomal or X-linked recessive inheritance rather than SCA6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_provenance.
- NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_assertion evidence source_evidence_literature NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_provenance.
- NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_assertion SIO_000772 12081723 NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_provenance.
- NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_assertion wasDerivedFrom befree-20140225 NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_provenance.
- NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_assertion wasGeneratedBy ECO_0000203 NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_provenance.