Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_assertion> ?p ?o ?g. }
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- NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_assertion type Assertion NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_head.
- NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_assertion wasGeneratedBy ECO_0000203 NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_provenance.
- NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_assertion wasDerivedFrom befree-20150227 NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_provenance.
- NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_assertion SIO_000772 21204806 NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_provenance.
- NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_assertion evidence source_evidence_literature NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_provenance.
- NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_assertion description "[The band 2q24 constitutes the smallest commonly deleted segment in these patients, and contains the voltage-gated sodium channel genes SCN1A and SCN2A, associated with Dravet syndrome and benign familial neonatal-infantile seizures, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682467.RA8ReWQKn4t7b7kNyn2GUhJG4cBBqgy0ADw2OqDUubIpE130_provenance.