Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_assertion> ?p ?o ?g. }
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- NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_assertion type Assertion NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_head.
- NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_assertion description "[To identify peripheral nerve abnormalities in hereditary spastic paraplegia (HSP) due to mutations in the spastin gene (spastic paraplegia 4, SPG4) using standard nerve conduction (NCS) and novel tests of axonal excitability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_provenance.
- NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_assertion evidence source_evidence_literature NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_provenance.
- NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_assertion SIO_000772 22192498 NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_provenance.
- NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_assertion wasDerivedFrom befree-2016 NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_provenance.
- NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_assertion wasGeneratedBy ECO_0000203 NP948674.RAKgIBm8LVBsgOFoUHiD2H1bPw1AyCGYLqge5Egdpj4OQ130_provenance.