Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_assertion type Assertion NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_head.
- NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_assertion description "[A high frequency (23%) of mutations in the peripherin/RDS gene was found in a cohort of 61 unrelated patients with various types of autosomal dominant central retinal dystrophies as compared with a low prevalence (1.3%) of mutations in this gene causing retinitis pigmentosa in a Spanish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_provenance.
- NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_assertion evidence source_evidence_literature NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_provenance.
- NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_assertion SIO_000772 17653047 NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_provenance.
- NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_assertion wasDerivedFrom befree-2016 NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_provenance.
- NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_assertion wasGeneratedBy ECO_0000203 NP621704.RAtL7ItuOsDEAhhcEdRO2QByMuI-EkH7BI5K9nk7jBMTI130_provenance.