Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_assertion> ?p ?o ?g. }
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- NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_assertion type Assertion NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_head.
- NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_assertion description "[Rett syndrome, a neurodevelopmental disorder caused by mutations in the X-linked gene encoding methyl-CpG-binding protein 2 (MeCP2), is a leading cause of mental retardation with autistic features in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_provenance.
- NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_assertion evidence source_evidence_literature NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_provenance.
- NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_assertion SIO_000772 16647848 NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_provenance.
- NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_assertion wasDerivedFrom befree-2016 NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_provenance.
- NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_assertion wasGeneratedBy ECO_0000203 NP547444.RAc7fYw7iArv3-o-3pK1IIzsXeep1mENo9bgl3Vd36s7E130_provenance.