Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_assertion type Assertion NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_head.
- NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_assertion description "[Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at least three genetic subtypes (USH2A, USH2B, and USH2C) and is classified phenotypically as congenital hearing loss and progressive retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.
- NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_assertion evidence source_evidence_literature NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.
- NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_assertion SIO_000772 14740321 NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.
- NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_assertion wasDerivedFrom befree-20140225 NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.
- NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_assertion wasGeneratedBy ECO_0000203 NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.