Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_assertion wasGeneratedBy ECO_0000218 NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_assertion wasDerivedFrom uniprot-20130724 NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_assertion SIO_000772 18625862 NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_assertion evidence source_evidence_curated NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_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." NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3761.RAYA8waOQ442uypE9AivMpKZnp8AlLdO2ohHcTF8RKdMs130_provenance.