Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_assertion> ?p ?o ?g. }
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- NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_assertion type Assertion NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_head.
- NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_assertion wasGeneratedBy ECO_0000203 NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_provenance.
- NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_assertion wasDerivedFrom befree-20140225 NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_provenance.
- NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_assertion SIO_000772 20186779 NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_provenance.
- NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_assertion evidence source_evidence_literature NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_provenance.
- NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_assertion description "[In one Iranian family segregating autosomal recessive non-syndromic hearing loss (ARNSHL), we identified a homozygous variant in a predicted miR-96/182 binding site in the 3'UTR of the RDX (DFNB24) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP249281.RAlZAC6z8oaRQfvpUqY69mXdLcr2d_uOizcR7izLk-Dzw130_provenance.