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- NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_assertion type Assertion NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_head.
- NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_assertion wasGeneratedBy ECO_0000218 NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_provenance.
- NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_assertion wasDerivedFrom uniprot-2016 NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_provenance.
- NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_assertion SIO_000772 16385458 NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_provenance.
- NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_assertion evidence source_evidence_curated NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_provenance.
- NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_assertion description "[Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_provenance.