Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_assertion> ?p ?o ?g. }
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- NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_assertion type Assertion NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_head.
- NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_assertion description "[The frequency for SPG4 mutations detected in autosomal dominant hereditary spastic paraplegia was 44.4%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_provenance.
- NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_assertion evidence source_evidence_literature NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_provenance.
- NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_assertion SIO_000772 16684598 NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_provenance.
- NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_assertion wasDerivedFrom befree-2016 NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_provenance.
- NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_assertion wasGeneratedBy ECO_0000203 NP548826.RAD6O6ffIX52hZBeO1rLVlsc7T6Yalvgeh27EgzbiNZs8130_provenance.