Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_assertion type Assertion NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_head.
- NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_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." NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_provenance.
- NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_assertion evidence source_evidence_literature NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_provenance.
- NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_assertion SIO_000772 9932941 NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_provenance.
- NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_assertion wasDerivedFrom befree-20140225 NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_provenance.
- NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_assertion wasGeneratedBy ECO_0000203 NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_provenance.