Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_assertion> ?p ?o ?g. }
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- NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_assertion type Assertion NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_head.
- NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_assertion description "[Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_provenance.
- NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_assertion evidence source_evidence_literature NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_provenance.
- NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_assertion SIO_000772 16648378 NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_provenance.
- NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_assertion wasDerivedFrom befree-20150227 NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_provenance.
- NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_assertion wasGeneratedBy ECO_0000203 NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_provenance.