Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_assertion type Assertion NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_head.
- NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_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." NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_provenance.
- NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_assertion evidence source_evidence_literature NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_provenance.
- NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_assertion SIO_000772 10704489 NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_provenance.
- NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_assertion wasDerivedFrom befree-20140225 NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_provenance.
- NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_assertion wasGeneratedBy ECO_0000203 NP860684.RAw1HoElhjNMkjqtjKff6fCy2knsJbQYMweI-fdVU15x8130_provenance.