Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_assertion> ?p ?o ?g. }
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- NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_assertion type Assertion NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_head.
- NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_provenance.
- NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_assertion evidence source_evidence_literature NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_provenance.
- NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_assertion SIO_000772 18978954 NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_provenance.
- NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_assertion wasDerivedFrom lhgdn-20090331 NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_provenance.
- NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_assertion wasGeneratedBy ECO_0000203 NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_provenance.