Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_assertion type Assertion NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_head.
- NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_assertion description "[Mutations in VLGRI in humans result in one form (2C) of Usher syndrome, the most common genetic cause of combined blindness and deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.
- NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_assertion evidence source_evidence_literature NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.
- NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_assertion SIO_000772 21618827 NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.
- NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_assertion wasDerivedFrom befree-20150227 NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.
- NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_assertion wasGeneratedBy ECO_0000203 NP954509.RAAbKJDOUzvLqTSOpa-E4Zp1cH1JBQk7zkiR0cHRI6zJg130_provenance.