Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_assertion type Assertion NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_head.
- NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_assertion wasGeneratedBy ECO_0000218 NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_provenance.
- NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_assertion wasDerivedFrom uniprot-2016 NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_provenance.
- NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_assertion SIO_000772 22004887 NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_provenance.
- NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_assertion evidence source_evidence_curated NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_provenance.
- NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_assertion description "[Considering only the patients clearly diagnosed with Usher syndrome type II, and results obtained in this and previous studies, we can state that mutations in USH2A are responsible for 76.1% of USH2 disease in patients of Spanish origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6817.RA4X813m4qfrCjwceCoPlfYkThmQr2Tqwl20JQwgW_2TM130_provenance.