Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_assertion> ?p ?o ?g. }
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- NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_assertion type Assertion NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_head.
- NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_assertion description "[Wagner syndrome (WGN1) is associated with mutations in versican (CSPG2) and snowflake vitreoretinal degeneration (SVD) with a mutation in a potassium channel (KCNJ13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_provenance.
- NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_assertion evidence source_evidence_literature NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_provenance.
- NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_assertion SIO_000772 18309337 NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_provenance.
- NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_assertion wasDerivedFrom befree-2016 NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_provenance.
- NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_assertion wasGeneratedBy ECO_0000203 NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_provenance.