Matches in Nanopublications for { <http://krauthammerlab.med.yale.edu/nanopub/GeneRIF272069.RAGbqSzBPkDXdbZwnBAZd7hPgM62fb_8_JxZhFN4_Jm9s#assertion> ?p ?o ?g. }
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- assertion type UnderspecifiedAssertion assertion.
- assertion asSentence Rett+syndrome+%28RTT%29+is+a+pervasive+development+disorder%2C+mainly+caused+by+mutations+in+the+methyl-CpG+binding+protein+2+%28MeCP2%29+gene. assertion.
- assertion wasDerivedFrom generifs_basic.gz provenance.
- assertion hadPrimarySource 21530498 provenance.
- assertion about 9606 assertion.
- assertion about 4204 assertion.