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- NP589494.RApk96T5X185iHvVRfBoyzyjjFbURP0i8_jKb4OTL4rMA130_assertion type Assertion NP589494.RApk96T5X185iHvVRfBoyzyjjFbURP0i8_jKb4OTL4rMA130_head.
- NP589494.RApk96T5X185iHvVRfBoyzyjjFbURP0i8_jKb4OTL4rMA130_assertion wasGeneratedBy ECO_0000203 NP589494.RApk96T5X185iHvVRfBoyzyjjFbURP0i8_jKb4OTL4rMA130_provenance.
- NP589494.RApk96T5X185iHvVRfBoyzyjjFbURP0i8_jKb4OTL4rMA130_assertion wasDerivedFrom befree-20140225 NP589494.RApk96T5X185iHvVRfBoyzyjjFbURP0i8_jKb4OTL4rMA130_provenance.
- NP589494.RApk96T5X185iHvVRfBoyzyjjFbURP0i8_jKb4OTL4rMA130_assertion SIO_000772 20186779 NP589494.RApk96T5X185iHvVRfBoyzyjjFbURP0i8_jKb4OTL4rMA130_provenance.
- NP589494.RApk96T5X185iHvVRfBoyzyjjFbURP0i8_jKb4OTL4rMA130_assertion evidence source_evidence_literature NP589494.RApk96T5X185iHvVRfBoyzyjjFbURP0i8_jKb4OTL4rMA130_provenance.
- NP589494.RApk96T5X185iHvVRfBoyzyjjFbURP0i8_jKb4OTL4rMA130_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." NP589494.RApk96T5X185iHvVRfBoyzyjjFbURP0i8_jKb4OTL4rMA130_provenance.