Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP676548.RAdBnlXO3ST3_qjWSGGyduPp7Pqf6765B7IHpbF_BhnMg#assertion> ?p ?o ?g. }
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- assertion description "[Rett syndrome (RTT), an X-linked dominant neurodevelopmental disorder in females, is caused mainly by de novo mutations in the methyl-CpG-binding protein 2 gene (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 21940684 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.