Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_provenance.
- NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_assertion description "[Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_provenance.
- NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_assertion evidence source_evidence_literature NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_provenance.
- NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_assertion SIO_000772 19089472 NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_provenance.
- NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_assertion wasDerivedFrom befree-20150227 NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_provenance.
- NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_assertion wasGeneratedBy ECO_0000203 NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_provenance.
- befree-20150227 importedOn "2015-02-27" NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_provenance.