Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_assertion> ?p ?o ?g. }
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- NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_assertion type Assertion NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_head.
- NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_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." NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_provenance.
- NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_assertion evidence source_evidence_literature NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_provenance.
- NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_assertion SIO_000772 9932941 NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_provenance.
- NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_assertion wasDerivedFrom befree-20140225 NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_provenance.
- NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_assertion wasGeneratedBy ECO_0000203 NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_provenance.