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- NP221920.RAe2jGZl5emfg0zvfBpe6bKjx3p1Yi7JOjL8_epMi8-6U130_assertion type Assertion NP221920.RAe2jGZl5emfg0zvfBpe6bKjx3p1Yi7JOjL8_epMi8-6U130_head.
- NP221920.RAe2jGZl5emfg0zvfBpe6bKjx3p1Yi7JOjL8_epMi8-6U130_assertion wasGeneratedBy ECO_0000203 NP221920.RAe2jGZl5emfg0zvfBpe6bKjx3p1Yi7JOjL8_epMi8-6U130_provenance.
- NP221920.RAe2jGZl5emfg0zvfBpe6bKjx3p1Yi7JOjL8_epMi8-6U130_assertion wasDerivedFrom befree-20150227 NP221920.RAe2jGZl5emfg0zvfBpe6bKjx3p1Yi7JOjL8_epMi8-6U130_provenance.
- NP221920.RAe2jGZl5emfg0zvfBpe6bKjx3p1Yi7JOjL8_epMi8-6U130_assertion SIO_000772 14684684 NP221920.RAe2jGZl5emfg0zvfBpe6bKjx3p1Yi7JOjL8_epMi8-6U130_provenance.
- NP221920.RAe2jGZl5emfg0zvfBpe6bKjx3p1Yi7JOjL8_epMi8-6U130_assertion evidence source_evidence_literature NP221920.RAe2jGZl5emfg0zvfBpe6bKjx3p1Yi7JOjL8_epMi8-6U130_provenance.
- NP221920.RAe2jGZl5emfg0zvfBpe6bKjx3p1Yi7JOjL8_epMi8-6U130_assertion description "[A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221920.RAe2jGZl5emfg0zvfBpe6bKjx3p1Yi7JOjL8_epMi8-6U130_provenance.