Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_assertion> ?p ?o ?g. }
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- NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_assertion type Assertion NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_head.
- NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_assertion description "[It is now clearly emerging that epilepsy has distinctive characteristics in typical Rett syndrome and in the different syndromes caused by CDKL5 and FOXG1 gene alterations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.
- NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_assertion evidence source_evidence_literature NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.
- NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_assertion SIO_000772 22998673 NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.
- NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_assertion wasDerivedFrom befree-2016 NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.
- NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_assertion wasGeneratedBy ECO_0000203 NP1014877.RAcRS6wYpPpfLHWRYcYlpD86MgvlOavcjfVxNvTX-f964130_provenance.