Matches in Nanopublications for { ?s ?p "[Mutations and deletions in the SPG4 gene are responsible for up to 40% of autosomal dominant hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations and deletions in the SPG4 gene are responsible for up to 40% of autosomal dominant hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations and deletions in the SPG4 gene are responsible for up to 40% of autosomal dominant hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_assertion description "[Mutations and deletions in the SPG4 gene are responsible for up to 40% of autosomal dominant hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_provenance.
- NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_assertion description "[Mutations and deletions in the SPG4 gene are responsible for up to 40% of autosomal dominant hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636940.RAxMTyD2fTg1jaqVSTFO5CWXHY2Mk7x5WmzgOz-3omohc130_provenance.