Matches in Nanopublications for { ?s ?p "[Rett syndrome, a neurodevelopmental disorder caused by mutations in the X-linked gene encoding methyl-CpG-binding protein 2 (MeCP2), is a leading cause of mental retardation with autistic features in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Rett syndrome, a neurodevelopmental disorder caused by mutations in the X-linked gene encoding methyl-CpG-binding protein 2 (MeCP2), is a leading cause of mental retardation with autistic features in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Rett syndrome, a neurodevelopmental disorder caused by mutations in the X-linked gene encoding methyl-CpG-binding protein 2 (MeCP2), is a leading cause of mental retardation with autistic features in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_assertion description "[Rett syndrome, a neurodevelopmental disorder caused by mutations in the X-linked gene encoding methyl-CpG-binding protein 2 (MeCP2), is a leading cause of mental retardation with autistic features in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_provenance.
- NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion description "[Rett syndrome, a neurodevelopmental disorder caused by mutations in the X-linked gene encoding methyl-CpG-binding protein 2 (MeCP2), is a leading cause of mental retardation with autistic features in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.