Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_assertion type Assertion NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_head.
- NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_assertion wasGeneratedBy ECO_0000203 NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_provenance.
- NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_assertion wasDerivedFrom befree-2016 NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_provenance.
- NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_assertion SIO_000772 8058286 NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_provenance.
- NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_assertion evidence source_evidence_literature NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_provenance.
- NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_assertion description "[Mutations in the human peripherin/retinal degeneration slow (rds) gene have been found in patients with macular dystrophies as well as in those with autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330988.RA4JjWgk39AOIPFzbKKIEJvUSZaZDDdhhqMjTERl6GVEo130_provenance.