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- source_evidence_literature type ECO_0000212 NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP840826.RAGKbeAIGrCpq0j82QaLjjIZgwaVNyf0ff3-cgwOg-FPE130_provenance.