Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_assertion> ?p ?o ?g. }
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- NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_assertion type Assertion NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_head.
- NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_assertion wasGeneratedBy ECO_0000203 NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_provenance.
- NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_assertion wasDerivedFrom lhgdn-20090331 NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_provenance.
- NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_assertion SIO_000772 16550584 NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_provenance.
- NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_assertion evidence source_evidence_literature NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_provenance.
- NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_assertion description "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_provenance.