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Matches in Nanopublications for
{ ?s ?p ?o <http://krauthammerlab.med.yale.edu/nanopub/GeneRIF272069.RAGbqSzBPkDXdbZwnBAZd7hPgM62fb_8_JxZhFN4_Jm9s#assertion>. }
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UnderspecifiedAssertion
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Rett+syndrome+%28RTT%29+is+a+pervasive+development+disorder%2C+mainly+caused+by+mutations+in+the+methyl-CpG+binding+protein+2+%28MeCP2%29+gene.
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9606
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4204
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