Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_assertion> ?p ?o ?g. }
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- NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_assertion type Assertion NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_head.
- NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_assertion wasGeneratedBy ECO_0000203 NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_provenance.
- NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_assertion wasDerivedFrom befree-20140225 NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_provenance.
- NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_assertion SIO_000772 21934280 NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_provenance.
- NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_assertion evidence source_evidence_literature NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_provenance.
- NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_assertion description "[Loss-of-function mutations of the MECP2 gene are the cause of most cases of Rett syndrome in females, a progressive neurodevelopmental disorder characterized by severe mental retardation, global regression, hand stereotypies, and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_provenance.