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- NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_assertion type Assertion NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_head.
- NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_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." NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_provenance.
- NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_assertion evidence source_evidence_literature NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_provenance.
- NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_assertion SIO_000772 18309337 NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_provenance.
- NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_assertion wasDerivedFrom befree-20140225 NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_provenance.
- NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_assertion wasGeneratedBy ECO_0000203 NP794549.RAvOrfuOeh4QU-wM3CJlXkBYuJqmbW7rTlXnqGqU-zZzM130_provenance.