Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_provenance.
- NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_assertion description "[Isovaleric acidemia (IVA) is a rare autosomal recessive disorder caused by a deficiency of isovaleryl-CoA dehydrogenase encoded by IVD gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_provenance.
- NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_assertion evidence source_evidence_literature NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_provenance.
- NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_assertion SIO_000772 23063737 NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_provenance.
- NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_assertion wasDerivedFrom befree-20140225 NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_provenance.
- NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_assertion wasGeneratedBy ECO_0000203 NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615016.RAKY2hXK2RCm393atZb8s4ouDKh79wyHhScROcZBkC5es130_provenance.