Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_assertion> ?p ?o ?g. }
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- NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_assertion type Assertion NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_head.
- NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_assertion wasGeneratedBy ECO_0000203 NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_provenance.
- NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_assertion wasDerivedFrom lhgdn-20090331 NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_provenance.
- NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_assertion SIO_000772 16550584 NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_provenance.
- NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_assertion evidence source_evidence_literature NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_provenance.
- NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_assertion description "[Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12), whereas null alleles cause the majority of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_provenance.