Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_assertion> ?p ?o ?g. }
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- NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_assertion type Assertion NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_head.
- NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_provenance.
- NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_assertion evidence source_evidence_literature NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_provenance.
- NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_assertion SIO_000772 12687499 NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_provenance.
- NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_assertion wasDerivedFrom befree-2016 NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_provenance.
- NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_assertion wasGeneratedBy ECO_0000203 NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_provenance.