Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_provenance.
- NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_assertion wasGeneratedBy ECO_0000218 NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_provenance.
- NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_assertion wasDerivedFrom uniprot-20130724 NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_provenance.
- NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_assertion SIO_000772 9452107 NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_provenance.
- NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_assertion evidence source_evidence_curated NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_provenance.
- NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_assertion description "[Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_provenance.