Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_assertion> ?p ?o ?g. }
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- NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_assertion type Assertion NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_head.
- NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_assertion description "[Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_provenance.
- NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_assertion evidence source_evidence_curated NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_provenance.
- NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_assertion SIO_000772 9328482 NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_provenance.
- NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_assertion wasDerivedFrom uniprot-2016 NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_provenance.
- NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_assertion wasGeneratedBy ECO_0000218 NP9520.RAX_xBtZLSZ-SlJzQ61QjKegm3yiZI25pFpJ34OwTCDJc130_provenance.