Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_assertion> ?p ?o ?g. }
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- NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_assertion type Assertion NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_head.
- NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_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." NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_provenance.
- NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_assertion evidence source_evidence_literature NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_provenance.
- NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_assertion SIO_000772 22998673 NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_provenance.
- NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_assertion wasDerivedFrom befree-20140225 NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_provenance.
- NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_assertion wasGeneratedBy ECO_0000203 NP316159.RAoDhxDom1oYsiLkHEFXvGfHH0OulR0A9JWyogLf0Zrl8130_provenance.