Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_assertion type Assertion NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_head.
- NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_assertion wasGeneratedBy ECO_0000218 NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_provenance.
- NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_assertion wasDerivedFrom uniprot-20130724 NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_provenance.
- NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_assertion SIO_000772 2018041 NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_provenance.
- NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_assertion evidence source_evidence_curated NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_provenance.
- NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_assertion description "[Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4204.RA3Jp1Bkco8MD6xKdv3HKsU7EBuC53qLvSdYnWT2VEpjY130_provenance.