Matches in Nanopublications for { ?s ?p "[Rett syndrome (RTT), an X-linked dominant neurodevelopmental disorder in females, is caused mainly by de novo mutations in the methyl-CpG-binding protein 2 gene (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_assertion description "[Rett syndrome (RTT), an X-linked dominant neurodevelopmental disorder in females, is caused mainly by de novo mutations in the methyl-CpG-binding protein 2 gene (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552186.RAa2EWLUKGMeJotHTepjw1X9OVDcs3ljKn0YD04H5xnCA130_provenance.
- assertion description "[Rett syndrome (RTT), an X-linked dominant neurodevelopmental disorder in females, is caused mainly by de novo mutations in the methyl-CpG-binding protein 2 gene (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_assertion description "[Rett syndrome (RTT), an X-linked dominant neurodevelopmental disorder in females, is caused mainly by de novo mutations in the methyl-CpG-binding protein 2 gene (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_provenance.
- NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_assertion description "[Rett syndrome (RTT), an X-linked dominant neurodevelopmental disorder in females, is caused mainly by de novo mutations in the methyl-CpG-binding protein 2 gene (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_provenance.
- NP925789.RAFgpuTbq5d10WY-fBNroPp5ArXUvY7vZZKT-FbnYEd1U130_assertion description "[Rett syndrome (RTT), an X-linked dominant neurodevelopmental disorder in females, is caused mainly by de novo mutations in the methyl-CpG-binding protein 2 gene (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925789.RAFgpuTbq5d10WY-fBNroPp5ArXUvY7vZZKT-FbnYEd1U130_provenance.