Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_provenance.
- NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_assertion description "[SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_provenance.
- NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_assertion evidence source_evidence_literature NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_provenance.
- NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_assertion SIO_000772 17301081 NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_provenance.
- NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_assertion wasDerivedFrom befree-20140225 NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_provenance.
- NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_assertion wasGeneratedBy ECO_0000203 NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_provenance.
- befree-20140225 importedOn "2014-02-25" NP610746.RAChtCbvtq9gGmjoXBUfdHor9xoes09jKiE7FNK6nsiao130_provenance.