Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_assertion> ?p ?o ?g. }
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- NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_assertion type Assertion NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_head.
- NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_assertion description "[Expressed ubiquitously and with some level of functional redundancy in most vital tissues, only one of the four genes--Atp2b2--has been causally linked through naturally occuring mutations to disease in mammals: specifically to deafness and ataxia in spontaneous mouse mutants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_provenance.
- NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_assertion evidence source_evidence_literature NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_provenance.
- NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_assertion SIO_000772 18193644 NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_provenance.
- NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_assertion wasDerivedFrom befree-20140225 NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_provenance.
- NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_assertion wasGeneratedBy ECO_0000203 NP513149.RAKhVbG4uyBQ1WUfDyu71vSr3ICPrguPxX7ySnc-CDrDE130_provenance.