Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP975112.RAQ57YiTmlf2fa61MwZr1dfvFkTRZG8GvJ85VV7TH6_yw#assertion> ?p ?o ?g. }
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- assertion description "[This study enables us to estimate the frequency of the SPG3A mutations in France at 39% in families with young-onset autosomal dominant spastic paraplegia after exclusion of SPG4 cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
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- assertion SIO_000772 15596607 provenance.
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