Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP658025.RAHqEkU29R4na-rGIH7PhzGKHlZpUElxrZs1zGbAfLANk130_provenance.