Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_assertion> ?p ?o ?g. }
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- NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_assertion type Assertion NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_head.
- NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_assertion wasGeneratedBy ECO_0000218 NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_provenance.
- NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_assertion wasDerivedFrom uniprot-20150221 NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_provenance.
- NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_assertion SIO_000772 18625862 NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_provenance.
- NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_assertion evidence source_evidence_curated NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_provenance.
- NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_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." NP614.RAlGDCH6Kq6aAllK1jc5H5BTACQiXO8veZkiZFlHqh4lI130_provenance.