Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_assertion> ?p ?o ?g. }
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- NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_assertion type Assertion NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_head.
- NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_assertion wasGeneratedBy ECO_0000203 NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_provenance.
- NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_assertion wasDerivedFrom befree-20150227 NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_provenance.
- NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_assertion SIO_000772 20642360 NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_provenance.
- NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_assertion evidence source_evidence_literature NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_provenance.
- NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_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." NP902776.RAEjAh9cUVKdhrNC5210a5jHC7CWkZlItQSlO6j2R7qMk130_provenance.