Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_provenance.
- NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_assertion description "[The most common Rhodopsin (Rh) mutation associated with autosomal dominant retinitis pigmentosa (ADRP) in North America is the substitution of proline 23 by histidine (Rh(P23H)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_provenance.
- NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_assertion evidence source_evidence_literature NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_provenance.
- NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_assertion SIO_000772 20865169 NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_provenance.
- NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_assertion wasDerivedFrom befree-2016 NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_provenance.
- NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_assertion wasGeneratedBy ECO_0000203 NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_provenance.
- befree-2016 importedOn "2016-02-19" NP841566.RAT4zg7OONLJ2BI16M6FB_XGGga4w6EloE1R7ozwgX6Bk130_provenance.