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- NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_assertion type Assertion NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_head.
- NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_assertion description "[Thus, we tested the hypothesis that a mutation within MYH9 is responsible for the autosomal dominant inheritance of MTCP and hearing loss in the Ghent family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_provenance.
- NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_assertion evidence source_evidence_literature NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_provenance.
- NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_assertion SIO_000772 19285578 NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_provenance.
- NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_assertion wasDerivedFrom befree-2016 NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_provenance.
- NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_assertion wasGeneratedBy ECO_0000203 NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_provenance.