Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_assertion> ?p ?o ?g. }
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- NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_assertion type Assertion NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_head.
- NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_assertion description "[Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_provenance.
- NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_assertion evidence source_evidence_curated NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_provenance.
- NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_assertion SIO_000772 23304067 NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_provenance.
- NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_assertion wasDerivedFrom uniprot-2016 NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_provenance.
- NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_assertion wasGeneratedBy ECO_0000218 NP7320.RAYpzmz1paFKSbQxonblrSNjS2TF3LPL_uqPtL9B2aRtI130_provenance.