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- NP226703.RAt6OU_SWxcN7cH1p3QH3DSjBXh-H3qZYnUt9GUIaXXHg130_assertion type Assertion NP226703.RAt6OU_SWxcN7cH1p3QH3DSjBXh-H3qZYnUt9GUIaXXHg130_head.
- NP226703.RAt6OU_SWxcN7cH1p3QH3DSjBXh-H3qZYnUt9GUIaXXHg130_assertion wasGeneratedBy ECO_0000203 NP226703.RAt6OU_SWxcN7cH1p3QH3DSjBXh-H3qZYnUt9GUIaXXHg130_provenance.
- NP226703.RAt6OU_SWxcN7cH1p3QH3DSjBXh-H3qZYnUt9GUIaXXHg130_assertion wasDerivedFrom befree-20140225 NP226703.RAt6OU_SWxcN7cH1p3QH3DSjBXh-H3qZYnUt9GUIaXXHg130_provenance.
- NP226703.RAt6OU_SWxcN7cH1p3QH3DSjBXh-H3qZYnUt9GUIaXXHg130_assertion SIO_000772 22735794 NP226703.RAt6OU_SWxcN7cH1p3QH3DSjBXh-H3qZYnUt9GUIaXXHg130_provenance.
- NP226703.RAt6OU_SWxcN7cH1p3QH3DSjBXh-H3qZYnUt9GUIaXXHg130_assertion evidence source_evidence_literature NP226703.RAt6OU_SWxcN7cH1p3QH3DSjBXh-H3qZYnUt9GUIaXXHg130_provenance.
- NP226703.RAt6OU_SWxcN7cH1p3QH3DSjBXh-H3qZYnUt9GUIaXXHg130_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." NP226703.RAt6OU_SWxcN7cH1p3QH3DSjBXh-H3qZYnUt9GUIaXXHg130_provenance.