Matches in Nanopublications for { ?s ?p "[Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP592201.RAAiJrOwhaZ17QF6cJXMVD38Twd0-NxBbpCTB0Ztfpy1g130_assertion description "[Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592201.RAAiJrOwhaZ17QF6cJXMVD38Twd0-NxBbpCTB0Ztfpy1g130_provenance.
- NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_assertion description "[Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_provenance.
- assertion description "[Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_assertion description "[Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_provenance.