Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_assertion> ?p ?o ?g. }
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- NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_assertion type Assertion NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_head.
- NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_assertion description "[The discovery of the c.1054C>T; p.R352W mutation in the FOXRED1 gene is a further contribution towards resolving the complex puzzle of the genetic basis of human mitochondrial disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_provenance.
- NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_assertion evidence source_evidence_literature NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_provenance.
- NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_assertion SIO_000772 20858599 NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_provenance.
- NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_assertion wasDerivedFrom befree-2016 NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_provenance.
- NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_assertion wasGeneratedBy ECO_0000203 NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_provenance.