Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion type Assertion NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_head.
- NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion evidence source_evidence_literature NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion SIO_000772 12687499 NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion wasDerivedFrom befree-20150227 NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion wasGeneratedBy ECO_0000203 NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.