Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_assertion> ?p ?o ?g. }
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- NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_assertion type Assertion NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_head.
- NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_assertion description "[Heterozygous mutations in BEST1 have previously been found to cause the two dominantly inherited disorders, Best macular dystrophy and autosomal-dominant vitreoretinochoroidopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_provenance.
- NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_assertion evidence source_evidence_literature NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_provenance.
- NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_assertion SIO_000772 18179881 NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_provenance.
- NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_assertion wasDerivedFrom befree-20150227 NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_provenance.
- NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_assertion wasGeneratedBy ECO_0000203 NP775464.RAvBbdcuCmtfrYBDvT0ZLrYwUjPL29JLdoTWWfQPXOzVE130_provenance.