Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_assertion> ?p ?o ?g. }
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- NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_assertion type Assertion NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_head.
- NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_assertion description "[Over the last several years, intragenic or genomic alterations of the CDKL5 and FOXG1 genes have been associated with severe cognitive impairment, early onset epilepsy and, often, dyskinetic movement disorders, which have variably been defined as Rett variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_provenance.
- NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_assertion evidence source_evidence_literature NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_provenance.
- NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_assertion SIO_000772 22998673 NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_provenance.
- NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_assertion wasDerivedFrom befree-20140225 NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_provenance.
- NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_assertion wasGeneratedBy ECO_0000203 NP773270.RAOjZvsASiD_u1G8Wl4nPojaCLA6_3lDSvLQwopj3ao74130_provenance.