Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_assertion> ?p ?o ?g. }
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- NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_assertion type Assertion NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_head.
- NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_assertion description "[Using fluorescent connexin fusion proteins, we show that the mutation induces a transport defect similar to that found for the Vohwinkel syndrome mutation p.Asp66His.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_provenance.
- NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_assertion evidence source_evidence_literature NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_provenance.
- NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_assertion SIO_000772 17993581 NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_provenance.
- NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_assertion wasDerivedFrom befree-20150227 NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_provenance.
- NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_assertion wasGeneratedBy ECO_0000203 NP1012249.RAkqSrSYtpiF34ElvaEWZWkj0eY2sb3YFc5KlK48T6lfI130_provenance.