Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_assertion> ?p ?o ?g. }
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- NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_assertion type Assertion NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_head.
- NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_assertion wasGeneratedBy ECO_0000203 NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_provenance.
- NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_assertion wasDerivedFrom befree-2016 NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_provenance.
- NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_assertion SIO_000772 16550584 NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_provenance.
- NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_assertion evidence source_evidence_literature NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_provenance.
- NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_assertion description "[Missense mutations within a defined region are associated with DFNA6/14/38, while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541237.RAz_gdLXdiLKK-ngLiIg4tcCkQqcsDmwYTFQHQWr3K9a8130_provenance.