Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion type Assertion NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_head.
- NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_provenance.
- NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion evidence source_evidence_curated NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_provenance.
- NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion SIO_000772 16384941 NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_provenance.
- NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion wasDerivedFrom ctd_human-20150221 NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_provenance.
- NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion wasGeneratedBy ECO_0000218 NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_provenance.