Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_assertion> ?p ?o ?g. }
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- NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_assertion type Assertion NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_head.
- NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_provenance.
- NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_assertion evidence source_evidence_literature NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_provenance.
- NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_assertion SIO_000772 10320095 NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_provenance.
- NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_assertion wasDerivedFrom befree-20140225 NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_provenance.
- NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_assertion wasGeneratedBy ECO_0000203 NP743665.RAi4axuJwVNsN7AHIGWaUjhUU0EoO9SrSEbvIAQLbnBZo130_provenance.