Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_assertion> ?p ?o ?g. }
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- NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_assertion type Assertion NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_head.
- NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_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." NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_provenance.
- NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_assertion evidence source_evidence_literature NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_provenance.
- NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_assertion SIO_000772 9932941 NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_provenance.
- NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_assertion wasDerivedFrom befree-20150227 NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_provenance.
- NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_assertion wasGeneratedBy ECO_0000203 NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_provenance.