Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_assertion> ?p ?o ?g. }
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- NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_assertion type Assertion NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_head.
- NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_assertion wasGeneratedBy ECO_0000203 NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_provenance.
- NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_assertion wasDerivedFrom befree-2016 NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_provenance.
- NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_assertion SIO_000772 12163457 NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_provenance.
- NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_assertion evidence source_evidence_literature NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_provenance.
- NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_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." NP363779.RAodCVdhv8Xa_X-dUJZcD4UVXYgy9cNrhr0MJAobGvx3w130_provenance.