Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_assertion> ?p ?o ?g. }
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- NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_assertion type Assertion NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_head.
- NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_assertion description "[Mutations in the human RDS gene are responsible for several forms of inherited blindness including autosomal-dominant retinitis pigmentosa and macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_provenance.
- NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_assertion evidence source_evidence_literature NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_provenance.
- NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_assertion SIO_000772 10704489 NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_provenance.
- NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_assertion wasDerivedFrom befree-2016 NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_provenance.
- NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_assertion wasGeneratedBy ECO_0000203 NP277191.RAsdCBJqbk3CXaejYg9PjogBMW0MeuB2-lmxwKuoCfHJY130_provenance.