Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_provenance.
- NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_assertion wasGeneratedBy ECO_0000218 NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_provenance.
- NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_assertion wasDerivedFrom uniprot-20130724 NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_provenance.
- NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_assertion SIO_000772 17296837 NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_provenance.
- NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_assertion evidence source_evidence_curated NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_provenance.
- NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_assertion description "[Two novel epilepsy-linked mutations leading to a loss of function of LGI1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3763.RAdTSXG_6Wlc3hqkf6LQev7bMEhJzU5Xrzdtx3rg9rVj0130_provenance.