Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_assertion> ?p ?o ?g. }
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- NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_assertion type Assertion NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_head.
- NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_assertion description "[A literature review of cases with chromosome 2q24.3 deletion revealed that, in most Dravet syndrome cases, it does not involve SCN2A and SCN3A, whereas a complex epilepsy phenotype that is shared with migrating partial seizures of infancy was associated with cases of deletion of the whole sodium channel gene cluster.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_provenance.
- NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_assertion evidence source_evidence_literature NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_provenance.
- NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_assertion SIO_000772 25524840 NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_provenance.
- NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_assertion wasDerivedFrom befree-2016 NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_provenance.
- NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_assertion wasGeneratedBy ECO_0000203 NP1249531.RA5ib15p-IP4n12nzYXKemwn8XfZf0iJkNG1SYHgwqX-o130_provenance.