Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP231907.RABlJiRQFYOm9OAwxcw63Wcw6e1h82k8wJ9gckKhSRD5E130_provenance.