Matches in Nanopublications for { ?s ?p "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_assertion description "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_provenance.
- NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_assertion description "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490589.RANl3ljUZU0yOLMCC9BF67lMQfFpMg4Dg12YNJxI3chW8130_provenance.
- assertion description "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_assertion description "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710144.RAHLgJJtRgXbjtVOtP8S_Vs3Y70ctBWSK0F2zRSPfwxS8130_provenance.
- NP262534.RAMECuvfUugjs7CFs0Un2orrdja-_roDFsWNdHsrdMbuE130_assertion description "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262534.RAMECuvfUugjs7CFs0Un2orrdja-_roDFsWNdHsrdMbuE130_provenance.
- NP710179.RA-o6DdARUEsrr3VT-JRSAQODqsNKW81W5JTmilOxme_Y130_assertion description "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710179.RA-o6DdARUEsrr3VT-JRSAQODqsNKW81W5JTmilOxme_Y130_provenance.
- NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_assertion description "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262535.RAxfvrqQKFlC6s1Y9B8LwgtUjBhbScIeZpH377U0bLfw0130_provenance.