Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_assertion> ?p ?o ?g. }
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- NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_assertion type Assertion NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_head.
- NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_assertion description "[Autosomal recessive ataxia with peripheral neuropathy and elevated AFP: novel mutations in SETX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.
- NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_assertion evidence source_evidence_literature NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.
- NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_assertion SIO_000772 16717225 NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.
- NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_assertion wasDerivedFrom befree-20150227 NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.
- NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_assertion wasGeneratedBy ECO_0000203 NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.