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- NP776951.RA3ZrKqJP5-0Eu7csXLt0fkblT4qlH2yORj4a9dNgeIdk130_assertion type Assertion NP776951.RA3ZrKqJP5-0Eu7csXLt0fkblT4qlH2yORj4a9dNgeIdk130_head.
- NP776951.RA3ZrKqJP5-0Eu7csXLt0fkblT4qlH2yORj4a9dNgeIdk130_assertion wasGeneratedBy ECO_0000203 NP776951.RA3ZrKqJP5-0Eu7csXLt0fkblT4qlH2yORj4a9dNgeIdk130_provenance.
- NP776951.RA3ZrKqJP5-0Eu7csXLt0fkblT4qlH2yORj4a9dNgeIdk130_assertion wasDerivedFrom befree-20150227 NP776951.RA3ZrKqJP5-0Eu7csXLt0fkblT4qlH2yORj4a9dNgeIdk130_provenance.
- NP776951.RA3ZrKqJP5-0Eu7csXLt0fkblT4qlH2yORj4a9dNgeIdk130_assertion SIO_000772 16550584 NP776951.RA3ZrKqJP5-0Eu7csXLt0fkblT4qlH2yORj4a9dNgeIdk130_provenance.
- NP776951.RA3ZrKqJP5-0Eu7csXLt0fkblT4qlH2yORj4a9dNgeIdk130_assertion evidence source_evidence_literature NP776951.RA3ZrKqJP5-0Eu7csXLt0fkblT4qlH2yORj4a9dNgeIdk130_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.