Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_assertion> ?p ?o ?g. }
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- NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_assertion type Assertion NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_head.
- NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_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." NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_provenance.
- NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_assertion evidence source_evidence_literature NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_provenance.
- NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_assertion SIO_000772 9932941 NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_provenance.
- NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_assertion wasDerivedFrom befree-20150227 NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_provenance.
- NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_assertion wasGeneratedBy ECO_0000203 NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_provenance.