Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_assertion> ?p ?o ?g. }
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- NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_assertion type Assertion NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_head.
- NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_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." NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_provenance.
- NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_assertion evidence source_evidence_literature NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_provenance.
- NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_assertion SIO_000772 22998673 NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_provenance.
- NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_assertion wasDerivedFrom befree-20150227 NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_provenance.
- NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_assertion wasGeneratedBy ECO_0000203 NP404348.RAEZYAZXoEhscwITVQnXXq32PBrB5rpn8R2K9qqwCp7Es130_provenance.