Matches in Nanopublications for { ?s ?p "[Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_assertion description "[Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_provenance.
- assertion description "[Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_assertion description "[Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_provenance.