Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_assertion type Assertion NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_head.
- NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_assertion wasGeneratedBy ECO_0000203 NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_provenance.
- NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_assertion wasDerivedFrom befree-2016 NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_provenance.
- NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_assertion SIO_000772 8058286 NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_provenance.
- NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_assertion evidence source_evidence_literature NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_provenance.
- NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_assertion description "[A previously undescribed mutation in the peripherin/rds gene is responsible for an autosomal dominant retinitis pigmentosa phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330984.RAp3CBH--dp8ZRZok5su_3Uz4EwSRS5KY0dXEumwvpf9M130_provenance.