Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_assertion> ?p ?o ?g. }
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- NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_assertion type Assertion NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_head.
- NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_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." NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_provenance.
- NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_assertion evidence source_evidence_literature NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_provenance.
- NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_assertion SIO_000772 9932941 NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_provenance.
- NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_assertion wasDerivedFrom befree-2016 NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_provenance.
- NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_assertion wasGeneratedBy ECO_0000203 NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_provenance.