Matches in Nanopublications for { ?s ?p "[Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutation of the X-linked MECP2 gene and characterized by developmental regression during the first few years of life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutation of the X-linked MECP2 gene and characterized by developmental regression during the first few years of life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_assertion description "[Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutation of the X-linked MECP2 gene and characterized by developmental regression during the first few years of life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293567.RAPasqhpxPrRs7ALfyU0jbcgAXKkGHPsYTxWhRaH1VegU130_provenance.