Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_assertion> ?p ?o ?g. }
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- NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_assertion type Assertion NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_head.
- NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_assertion wasGeneratedBy ECO_0000203 NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_provenance.
- NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_assertion wasDerivedFrom befree-20150227 NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_provenance.
- NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_assertion SIO_000772 22735794 NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_provenance.
- NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_assertion evidence source_evidence_literature NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_provenance.
- NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_assertion description "[The aim of this study was to identify mutations in the TRPM1, GRM6, NYX and CACNA1F genes in patients with congenital stationary night blindness (CSNB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435759.RAqgscbnuVxV89EUn5crxpVJ3zq8ldLjXltnWNOCYeQOw130_provenance.