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- NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_assertion type Assertion NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_head.
- NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_assertion wasGeneratedBy ECO_0000203 NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.
- NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_assertion wasDerivedFrom befree-2016 NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.
- NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_assertion SIO_000772 21241800 NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.
- NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_assertion evidence source_evidence_literature NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.
- NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_assertion description "[Biophysical properties of mutant KCNQ1 S277L channels linked to hereditary long QT syndrome with phenotypic variability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865816.RAAbpcO8NV2L2a7wv0L-_3LHly-YTtSHdGo3ZpbCOIWO8130_provenance.