Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_assertion> ?p ?o ?g. }
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- NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_assertion type Assertion NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_head.
- NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_assertion wasGeneratedBy ECO_0000203 NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_provenance.
- NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_assertion wasDerivedFrom befree-2016 NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_provenance.
- NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_assertion SIO_000772 18625862 NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_provenance.
- NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_assertion evidence source_evidence_literature NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_provenance.
- NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_assertion description "[A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_provenance.