Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion type Assertion NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_head.
- NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion evidence source_evidence_literature NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion SIO_000772 10612833 NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion wasDerivedFrom befree-2016 NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion wasGeneratedBy ECO_0000203 NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.