Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_assertion> ?p ?o ?g. }
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- NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_assertion type Assertion NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_head.
- NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_assertion wasGeneratedBy ECO_0000218 NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_provenance.
- NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_assertion wasDerivedFrom uniprot-2016 NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_provenance.
- NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_assertion SIO_000772 18625862 NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_provenance.
- NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_assertion evidence source_evidence_curated NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_provenance.
- NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_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." NP5449.RAlJTPGKTGatZ86J0I68IfdEtvaiXaJNM6VWsdo_BSmcs130_provenance.