Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_assertion> ?p ?o ?g. }
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- NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_assertion type Assertion NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_head.
- NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_assertion description "[HeLa cells stably expressing nine dominant Cx26 mutants, six associated with non-syndromic hearing loss (W44C, W44S, R143Q, D179N, R184Q and C202F) and three associated with hearing loss and palmoplantar keratoderma (G59A, R75Q and R75W), individually or together with Cx30, were analyzed by immunocytochemistry, co-immunoprecipitation, and functional assays (scrape-loading and/or fluorescence recovery after photobleaching).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_provenance.
- NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_assertion evidence source_evidence_literature NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_provenance.
- NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_assertion SIO_000772 20096356 NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_provenance.
- NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_assertion wasDerivedFrom befree-2016 NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_provenance.
- NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_assertion wasGeneratedBy ECO_0000203 NP788881.RA1t6cs5UHh68WVtKEaP4hj_OtpvmzO3CvrliE7p8IXTc130_provenance.