Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_assertion> ?p ?o ?g. }
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- NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_assertion type Assertion NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_head.
- NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_assertion description "[The authors identified a novel peripherin/RDS gene mutation associated with autosomal dominant retinal degeneration in patients from three different families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_provenance.
- NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_assertion evidence source_evidence_literature NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_provenance.
- NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_assertion SIO_000772 7862413 NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_provenance.
- NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_assertion wasDerivedFrom befree-2016 NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_provenance.
- NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_assertion wasGeneratedBy ECO_0000203 NP1324177.RAI8tvW7BOuWyGM21_iQDHe2uoeRB35urg0EtQX4WB7lk130_provenance.