Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_provenance.
- NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_assertion wasGeneratedBy ECO_0000218 NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_provenance.
- NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_assertion wasDerivedFrom uniprot-2016 NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_provenance.
- NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_assertion SIO_000772 15776429 NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_provenance.
- NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_assertion evidence source_evidence_curated NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_provenance.
- NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_assertion description "[Recently, SIMPLE/LITAF was shown to be responsible for an autosomal dominant demyelinating form of CMT linked to 16p (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3952.RAQy2lKzHUvNP5tkaVIAPfyHzc2SKdjzXhZ73_hWaPm5g130_provenance.