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- NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_assertion type Assertion NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_head.
- NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_assertion wasGeneratedBy ECO_0000203 NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_provenance.
- NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_assertion wasDerivedFrom befree-2016 NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_provenance.
- NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_assertion SIO_000772 8045710 NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_provenance.
- NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_assertion evidence source_evidence_literature NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_provenance.
- NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_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." NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_provenance.