Matches in Nanopublications for { ?s ?p "[Similarly, allelsim in the gene encoding wolframin (WFS1) causes either a nonsyndromic dominant low-frequency hearing loss (DFNA6/14/38) or Wolfram syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP198423.RACu-TS22Os8mF_imz2NzvBoffMumvP8BafYlFURt8kAU130_assertion description "[Similarly, allelsim in the gene encoding wolframin (WFS1) causes either a nonsyndromic dominant low-frequency hearing loss (DFNA6/14/38) or Wolfram syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198423.RACu-TS22Os8mF_imz2NzvBoffMumvP8BafYlFURt8kAU130_provenance.
- NP776951.RA3ZrKqJP5-0Eu7csXLt0fkblT4qlH2yORj4a9dNgeIdk130_assertion description "[Similarly, allelsim in the gene encoding wolframin (WFS1) causes either a nonsyndromic dominant low-frequency hearing loss (DFNA6/14/38) or Wolfram syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776951.RA3ZrKqJP5-0Eu7csXLt0fkblT4qlH2yORj4a9dNgeIdk130_provenance.
- NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_assertion description "[Similarly, allelsim in the gene encoding wolframin (WFS1) causes either a nonsyndromic dominant low-frequency hearing loss (DFNA6/14/38) or Wolfram syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.