Matches in Nanopublications for { ?s ?p "[Similarly, ATP1A3 mutations cause a wide phenotypic spectrum ranging from rapid-onset dystonia-parkinsonism to alternating hemiplegia of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Similarly, ATP1A3 mutations cause a wide phenotypic spectrum ranging from rapid-onset dystonia-parkinsonism to alternating hemiplegia of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Similarly, ATP1A3 mutations cause a wide phenotypic spectrum ranging from rapid-onset dystonia-parkinsonism to alternating hemiplegia of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_assertion description "[Similarly, ATP1A3 mutations cause a wide phenotypic spectrum ranging from rapid-onset dystonia-parkinsonism to alternating hemiplegia of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_provenance.
- NP1260240.RAUVyg-aKoAJTQG9igWRIUrz_CVu9w8hZDGkVzkDvAY9A130_assertion description "[Similarly, ATP1A3 mutations cause a wide phenotypic spectrum ranging from rapid-onset dystonia-parkinsonism to alternating hemiplegia of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260240.RAUVyg-aKoAJTQG9igWRIUrz_CVu9w8hZDGkVzkDvAY9A130_provenance.