Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_assertion type Assertion NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_head.
- NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_assertion description "[We have recently shown, with others, that mutations in the OPA1 gene encoding a dynamin-related mitochondrial protein, underlie the dominant form of optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_provenance.
- NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_assertion evidence source_evidence_literature NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_provenance.
- NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_assertion SIO_000772 11810270 NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_provenance.
- NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_assertion wasDerivedFrom befree-20140225 NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_provenance.
- NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_assertion wasGeneratedBy ECO_0000203 NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_provenance.