Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_assertion> ?p ?o ?g. }
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- NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_assertion type Assertion NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_head.
- NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_assertion wasGeneratedBy ECO_0000218 NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_provenance.
- NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_assertion wasDerivedFrom uniprot-20130724 NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_provenance.
- NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_assertion SIO_000772 12163457 NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_provenance.
- NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_assertion evidence source_evidence_curated NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_provenance.
- NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_assertion description "[Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3451.RATR8wkOnXTSDbR4hMAyydOCLJ0q9yS81HiIlHVwc-phs130_provenance.