Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_assertion> ?p ?o ?g. }
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- NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_assertion type Assertion NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_head.
- NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_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." NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_provenance.
- NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_assertion evidence source_evidence_literature NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_provenance.
- NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_assertion SIO_000772 22998673 NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_provenance.
- NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_assertion wasDerivedFrom befree-20140225 NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_provenance.
- NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_assertion wasGeneratedBy ECO_0000203 NP866842.RAREoc0AImas4VkG6yQY0ul7NaONpL6rvYLkfe8J8DHuI130_provenance.