Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_assertion> ?p ?o ?g. }
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- NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_assertion type Assertion NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_head.
- NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_provenance.
- NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_assertion evidence source_evidence_literature NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_provenance.
- NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_assertion SIO_000772 10502787 NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_provenance.
- NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_assertion wasDerivedFrom befree-2016 NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_provenance.
- NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_assertion wasGeneratedBy ECO_0000203 NP264321.RAAE_KyabMXvECVElSCspw9V3hImnZlWDXxiLpBdzSXCg130_provenance.