Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_assertion> ?p ?o ?g. }
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- NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_assertion type Assertion NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_head.
- NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_assertion wasGeneratedBy ECO_0000203 NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_provenance.
- NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_assertion wasDerivedFrom befree-20140225 NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_provenance.
- NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_assertion SIO_000772 20642360 NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_provenance.
- NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_assertion evidence source_evidence_literature NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_provenance.
- NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_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." NP161425.RAtlABeLyhwzZ1uDpiV-Pn8LPCkiNtoVa2Ia5RhP87PEk130_provenance.