Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_assertion> ?p ?o ?g. }
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- NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_assertion type Assertion NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_head.
- NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_assertion wasGeneratedBy ECO_0000203 NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.
- NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_assertion wasDerivedFrom befree-2016 NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.
- NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_assertion SIO_000772 16550584 NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_provenance.
- NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_assertion evidence source_evidence_literature NP541239.RA35ZKNIU-15BJyfJKyShRH-0Bf-FbWiYMQDkyyB7gA50130_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.