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- NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_assertion type Assertion NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_head.
- NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_assertion wasGeneratedBy ECO_0000203 NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_provenance.
- NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_assertion wasDerivedFrom befree-20140225 NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_provenance.
- NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_assertion SIO_000772 8045710 NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_provenance.
- NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_assertion evidence source_evidence_literature NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_provenance.
- NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_provenance.