Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_assertion> ?p ?o ?g. }
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- NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_assertion type Assertion NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_head.
- NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_assertion wasGeneratedBy ECO_0000203 NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_provenance.
- NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_assertion wasDerivedFrom befree-20140225 NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_provenance.
- NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_assertion SIO_000772 8045710 NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_provenance.
- NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_assertion evidence source_evidence_literature NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_provenance.
- NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_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." NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_provenance.