Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_provenance.
- befree-2016 importedOn "2016-02-19" NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_provenance.
- NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_assertion wasGeneratedBy ECO_0000203 NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_provenance.
- NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_assertion wasDerivedFrom befree-2016 NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_provenance.
- NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_assertion SIO_000772 15009222 NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_provenance.
- NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_assertion evidence source_evidence_literature NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_provenance.
- NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_assertion description "[Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434819.RAA5qC_51xht-niyz9ptWoO8HmdbAEp9WAABGUP7xatKI130_provenance.