Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_provenance.
- NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_assertion description "[Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_provenance.
- NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_assertion evidence source_evidence_curated NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_provenance.
- NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_assertion SIO_000772 11810107 NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_provenance.
- NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_assertion wasDerivedFrom uniprot-20150221 NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_provenance.
- NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_assertion wasGeneratedBy ECO_0000218 NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP612.RAZ4yG3KqsFCCjn0hcAGwWDSb0-Uac9gtM8GhN3gyqTqo130_provenance.