Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_provenance.
- NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_assertion description "[Furthermore, during the last decade, it has been identified that mutations in two mitochondrial fusion genes (MFN2 and OPA1) cause prevalent neurodegenerative diseases (Charcot-Marie Tooth type 2A and Kjer disease/autosomal dominant optic atrophy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_provenance.
- NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_assertion evidence source_evidence_literature NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_provenance.
- NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_assertion SIO_000772 19584314 NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_provenance.
- NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_assertion wasDerivedFrom befree-2016 NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_provenance.
- NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_assertion wasGeneratedBy ECO_0000203 NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_provenance.
- befree-2016 importedOn "2016-02-19" NP749985.RAN9Z_C5yQR0uA_zY8E2e0lY1lG2o5HLhD97myFeJ_bvM130_provenance.