Matches in Nanopublications for { ?s ?p "[Mutations in MECP2, encoding methyl CpG binding protein 2 (MeCP2), cause most cases of Rett syndrome (RTT), an X-linked neurodevelopmental disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_assertion description "[Mutations in MECP2, encoding methyl CpG binding protein 2 (MeCP2), cause most cases of Rett syndrome (RTT), an X-linked neurodevelopmental disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_provenance.
- NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_assertion description "[Mutations in MECP2, encoding methyl CpG binding protein 2 (MeCP2), cause most cases of Rett syndrome (RTT), an X-linked neurodevelopmental disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608748.RAKCRo5SADnneEiOW5yUp0O_lywJERivJN2uYMTJoGFRc130_provenance.