Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_provenance.
- NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_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." NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_provenance.
- NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_assertion evidence source_evidence_literature NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_provenance.
- NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_assertion SIO_000772 19584314 NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_provenance.
- NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_assertion wasDerivedFrom befree-20150227 NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_provenance.
- NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_assertion wasGeneratedBy ECO_0000203 NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP833410.RAI4PA5u5qAuXg-Pi4qkWGnCa39kXQwt4L49T50s24Sjg130_provenance.