Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_provenance.
- befree-2016 importedOn "2016-02-19" NP682048.RAaNB1PIFjhv1TnkUtc54bwZu8iiBhYXqvutea8-iJQHY130_provenance.
- 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.