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- NP237116.RA9h-rEQ2ByAitMzCgb8oisOOkLadlg-yCbbqdOIbsjbs130_assertion type Assertion NP237116.RA9h-rEQ2ByAitMzCgb8oisOOkLadlg-yCbbqdOIbsjbs130_head.
- NP237116.RA9h-rEQ2ByAitMzCgb8oisOOkLadlg-yCbbqdOIbsjbs130_assertion wasGeneratedBy ECO_0000203 NP237116.RA9h-rEQ2ByAitMzCgb8oisOOkLadlg-yCbbqdOIbsjbs130_provenance.
- NP237116.RA9h-rEQ2ByAitMzCgb8oisOOkLadlg-yCbbqdOIbsjbs130_assertion wasDerivedFrom befree-20150227 NP237116.RA9h-rEQ2ByAitMzCgb8oisOOkLadlg-yCbbqdOIbsjbs130_provenance.
- NP237116.RA9h-rEQ2ByAitMzCgb8oisOOkLadlg-yCbbqdOIbsjbs130_assertion SIO_000772 20357205 NP237116.RA9h-rEQ2ByAitMzCgb8oisOOkLadlg-yCbbqdOIbsjbs130_provenance.
- NP237116.RA9h-rEQ2ByAitMzCgb8oisOOkLadlg-yCbbqdOIbsjbs130_assertion evidence source_evidence_literature NP237116.RA9h-rEQ2ByAitMzCgb8oisOOkLadlg-yCbbqdOIbsjbs130_provenance.
- NP237116.RA9h-rEQ2ByAitMzCgb8oisOOkLadlg-yCbbqdOIbsjbs130_assertion description "[Common mutations for Leber's hereditary optic neuropathy (LHON: G11778A; T14484C; and G3460A) were not present in AMD samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237116.RA9h-rEQ2ByAitMzCgb8oisOOkLadlg-yCbbqdOIbsjbs130_provenance.