Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_assertion> ?p ?o ?g. }
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- NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_assertion type Assertion NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_head.
- NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_provenance.
- NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_assertion evidence source_evidence_literature NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_provenance.
- NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_assertion SIO_000772 23941260 NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_provenance.
- NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_assertion wasDerivedFrom befree-20150227 NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_provenance.
- NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_assertion wasGeneratedBy ECO_0000203 NP867821.RAN6yHK4dnu58nDHwlYv0SDjwI9STe6wllfy31Yar3udY130_provenance.