Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_assertion type Assertion NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_head.
- NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_assertion description "[To clinically characterize a Swedish family with autosomal dominant retinitis pigmentosa due to a mutation, Arg-172-Trp, in the peripherin/RDS gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_provenance.
- NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_assertion evidence source_evidence_literature NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_provenance.
- NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_assertion SIO_000772 9810570 NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_provenance.
- NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_assertion wasDerivedFrom befree-2016 NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_provenance.
- NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_assertion wasGeneratedBy ECO_0000203 NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_provenance.