Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_provenance.
- NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_assertion description "[Depending on the clinical and biochemical phenotype we suggest POLG1, SUCLA2, TMEM70 and RYR1 sequence analysis and mtDNA-depletion studies in children with 3-methylglutaconic aciduria type IV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_provenance.
- NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_assertion evidence source_evidence_literature NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_provenance.
- NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_assertion SIO_000772 19015156 NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_provenance.
- NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_assertion wasDerivedFrom befree-20140225 NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_provenance.
- NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_assertion wasGeneratedBy ECO_0000203 NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP833851.RAx5eJ9Z0NGZThCLb4OUancUKC0iNJ1NX3KByDJgmKDEE130_provenance.