Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_assertion> ?p ?o ?g. }
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- NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_assertion type Assertion NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_head.
- NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_assertion wasGeneratedBy ECO_0000203 NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_provenance.
- NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_assertion wasDerivedFrom befree-20140225 NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_provenance.
- NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_assertion SIO_000772 16550584 NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_provenance.
- NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_assertion evidence source_evidence_literature NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_provenance.
- NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_assertion description "[Missense mutations in CDH23 have been associated with presbycusis and DFNB12, whereas null alleles cause the majority of Usher 1D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720207.RAEK7wMp4Owv5qHRVo8qUYoK7ajnRlrFOlC0eM7LJWOI4130_provenance.