Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_assertion> ?p ?o ?g. }
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- NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_assertion type Assertion NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_head.
- NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_assertion description "[Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_provenance.
- NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_assertion evidence source_evidence_curated NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_provenance.
- NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_assertion SIO_000772 10973849 NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_provenance.
- NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_assertion wasDerivedFrom uniprot-2016 NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_provenance.
- NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_assertion wasGeneratedBy ECO_0000218 NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_provenance.