Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_provenance.
- NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_assertion description "[Mutations in the TMEM70 gene are the most common cause of nuclear encoded ATP synthase deficiency resulting in a syndrome characterized by neonatal lactic acidosis, cardiomyopathy, and encephalomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_provenance.
- NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_assertion evidence source_evidence_literature NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_provenance.
- NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_assertion SIO_000772 23235116 NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_provenance.
- NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_assertion wasDerivedFrom befree-20140225 NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_provenance.
- NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_assertion wasGeneratedBy ECO_0000203 NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_provenance.