Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_assertion type Assertion NP4215.RARl3dSn_bbK_4jwb3jlvByE-k0KdJGYWQq3lVDNVNqGU130_head.
- 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.