Matches in Nanopublications for { ?s ?p "[Rett syndrome (RTT) is an X-linked neurodevelopmental disorder linked to heterozygous de novo mutations in the MECP2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_assertion description "[Rett syndrome (RTT) is an X-linked neurodevelopmental disorder linked to heterozygous de novo mutations in the MECP2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246321.RA54nuMgldi6EiD2EDFVmwPwDhLA-XfHWBm3suqahErJM130_provenance.
- assertion description "[Rett syndrome (RTT) is an X-linked neurodevelopmental disorder linked to heterozygous de novo mutations in the MECP2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_assertion description "[Rett syndrome (RTT) is an X-linked neurodevelopmental disorder linked to heterozygous de novo mutations in the MECP2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP594731.RAG5nlooj_VxC9jcYsdxzHanUQSnmbnShe1GtG8fVyfWY130_provenance.