Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_assertion> ?p ?o ?g. }
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- NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_assertion type Assertion NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_head.
- NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_assertion description "[The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_provenance.
- NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_assertion evidence source_evidence_curated NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_provenance.
- NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_assertion SIO_000772 10732799 NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_provenance.
- NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_assertion wasDerivedFrom uniprot-2016 NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_provenance.
- NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_assertion wasGeneratedBy ECO_0000218 NP701.RAbBU-EWSP9N4P0eYI4t7lXxCaBdHEkXbcDWw8gjWop8Y130_provenance.