Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_assertion type Assertion NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_head.
- NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_assertion description "[The major clinical features of SPTAN1 mutations include epileptic encephalopathy with hypsarrhythmia, no visual attention, acquired microcephaly, spastic quadriplegia and severe intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_provenance.
- NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_assertion evidence source_evidence_literature NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_provenance.
- NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_assertion SIO_000772 25631096 NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_provenance.
- NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_assertion wasDerivedFrom befree-2016 NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_provenance.
- NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_assertion wasGeneratedBy ECO_0000203 NP1259186.RAQeK2D_hH76I8CkaJi81fbBhWoWb3a3tDYXzsnCXbFGg130_provenance.