Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_provenance.
- 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.
- uniprot-2016 importedOn "2016-01-25" NP1006.RAbdpL9WuiIJiCr4NHUjBT4xwXET9IN0K8loK1RvE5smY130_provenance.