Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_assertion> ?p ?o ?g. }
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- NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_assertion type Assertion NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_head.
- NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_assertion description "[These results confirm the association of the MTND6*LDYT14459A mutation with Leber's hereditary optic neuropathy and/or dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_provenance.
- NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_assertion evidence source_evidence_literature NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_provenance.
- NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_assertion SIO_000772 7654063 NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_provenance.
- NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_assertion wasDerivedFrom befree-20140225 NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_provenance.
- NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_assertion wasGeneratedBy ECO_0000203 NP341018.RAh2Klffxdf1mTkv2LRLGqh6hhdStnolGL8MSH9Y4-6JM130_provenance.