Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_assertion> ?p ?o ?g. }
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- NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_assertion type Assertion NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_head.
- NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_assertion description "[Mutant alleles of a third unconventional myosin, myosin XV, are associated with nonsyndromic, recessive, congenital deafness DFNB3 on human chromosome 17p11.2 and deafness in shaker2 (Myo15(sh2)) mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_provenance.
- NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_assertion evidence source_evidence_literature NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_provenance.
- NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_assertion SIO_000772 10704189 NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_provenance.
- NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_assertion wasDerivedFrom befree-20140225 NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_provenance.
- NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_assertion wasGeneratedBy ECO_0000203 NP823472.RA4xmpwZymu9f2QZAu0PwIP0TnkBdar2xQLhtwVEHbqJ8130_provenance.