Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_provenance.
- NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_assertion description "[Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_provenance.
- NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_assertion evidence source_evidence_curated NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_provenance.
- NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_assertion SIO_000772 20206331 NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_provenance.
- NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_assertion wasDerivedFrom uniprot-20130724 NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_provenance.
- NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_assertion wasGeneratedBy ECO_0000218 NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP6195.RAQr8A-2SyeF0aBlqn6EznDNLOyGXzASvE8dlsEQXaOOM130_provenance.