Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_assertion> ?p ?o ?g. }
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- NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_assertion type Assertion NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_head.
- NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_assertion description "[It has recently been shown that mutations in RDH12, encoding a retinol dehydrogenase, result in severe and early-onset autosomal recessive retinal dystrophy (arRD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_provenance.
- NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_assertion evidence source_evidence_literature NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_provenance.
- NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_assertion SIO_000772 16269441 NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_provenance.
- NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_assertion wasDerivedFrom befree-20140225 NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_provenance.
- NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_assertion wasGeneratedBy ECO_0000203 NP642077.RABMeticHGsPHwGVSJDHUW_utYhUdaMOCTMdVBQbVYlhA130_provenance.