Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_assertion> ?p ?o ?g. }
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- NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_assertion type Assertion NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_head.
- NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_assertion description "[Other vitreoretinal degenerations including a number of chondrodysplasias in addition to STL1 and STL2, enhanced S-cone syndrome caused by mutations in NR2E3, and autosomal dominant vitreoretinochoroidopathy caused by mutations in VMD2 are discussed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_provenance.
- NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_assertion evidence source_evidence_literature NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_provenance.
- NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_assertion SIO_000772 18309337 NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_provenance.
- NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_assertion wasDerivedFrom befree-20150227 NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_provenance.
- NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_assertion wasGeneratedBy ECO_0000203 NP319519.RAwN0qFVYVJv0l3vECQTGICaT3aFYabe98IWv7WJPLeMo130_provenance.