Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_assertion> ?p ?o ?g. }
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- NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_assertion type Assertion NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_head.
- NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_assertion wasGeneratedBy ECO_0000203 NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_provenance.
- NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_assertion wasDerivedFrom befree-20140225 NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_provenance.
- NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_assertion SIO_000772 20642360 NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_provenance.
- NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_assertion evidence source_evidence_literature NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_provenance.
- NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_assertion description "[We estimate the prevalence of homozygous MYO15A mutations in autosomal recessive nonsyndromic deafness in Turkey as 0.062 (95% confidence interval is 0.020-0.105).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368733.RAVwAKr6hUHmsfUiuk6DFfpeav3mr7A2ELifSkXTZXK4o130_provenance.