Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_assertion> ?p ?o ?g. }
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- NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_assertion type Assertion NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_head.
- NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_assertion wasGeneratedBy ECO_0000203 NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_provenance.
- NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_assertion wasDerivedFrom befree-2016 NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_provenance.
- NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_assertion SIO_000772 23372056 NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_provenance.
- NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_assertion evidence source_evidence_literature NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_provenance.
- NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_assertion description "[Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1049082.RAQ8UAaB87LQb5sTPsfVQPudZTX01NmT6OQOWYb9KNXuA130_provenance.