Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_provenance.