Matches in Nanopublications for { ?s ?p "[Rett syndrome (RTT) is a neurodevelopmental disorder mostly caused by MECP2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion description "[Rett syndrome (RTT) is a neurodevelopmental disorder mostly caused by MECP2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.