Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_assertion> ?p ?o ?g. }
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- NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_assertion type Assertion NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_head.
- NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_assertion description "[The largest homozygous region (~11 Mb) in the affected family members was mapped to chromosome 9, which harbors deafness, autosomal recessive 31 (DFNB31; a gene previously associated with Usher syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_provenance.
- NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_assertion evidence source_evidence_literature NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_provenance.
- NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_assertion SIO_000772 21738389 NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_provenance.
- NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_assertion wasDerivedFrom befree-20150227 NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_provenance.
- NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_assertion wasGeneratedBy ECO_0000203 NP879386.RAq7i-7Tlw7IMbMR97eFYk_v8NSMqoBh3cjTd3hMy8erQ130_provenance.