Matches in Nanopublications for { ?s ?p "[Loss of CSTB function due to mutations is consistent with the observed neurodegenerative pathology and phenotype, but the functional link to the epileptic phenotype of EPM1 remains largely unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_assertion description "[Loss of CSTB function due to mutations is consistent with the observed neurodegenerative pathology and phenotype, but the functional link to the epileptic phenotype of EPM1 remains largely unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_provenance.
- assertion description "[Loss of CSTB function due to mutations is consistent with the observed neurodegenerative pathology and phenotype, but the functional link to the epileptic phenotype of EPM1 remains largely unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_assertion description "[Loss of CSTB function due to mutations is consistent with the observed neurodegenerative pathology and phenotype, but the functional link to the epileptic phenotype of EPM1 remains largely unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_provenance.
- NP415748.RAVUzWkk7XtuuqF006Bx4aXtkxT48pxlHuVJt6GHE9qAY130_assertion description "[Loss of CSTB function due to mutations is consistent with the observed neurodegenerative pathology and phenotype, but the functional link to the epileptic phenotype of EPM1 remains largely unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415748.RAVUzWkk7XtuuqF006Bx4aXtkxT48pxlHuVJt6GHE9qAY130_provenance.
- NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_assertion description "[Loss of CSTB function due to mutations is consistent with the observed neurodegenerative pathology and phenotype, but the functional link to the epileptic phenotype of EPM1 remains largely unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415744.RAg4mw8YK_Ee-Sxkx3hHz_VUDs_LKA--F5aHjndMIoDk4130_provenance.