Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP862161.RAZmOGZUYd-ME5eCmKiE9WuWcUiXQP_DPU5YovftSUFxg#assertion> ?p ?o ?g. }
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- assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 9932941 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.