Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_assertion> ?p ?o ?g. }
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- NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_assertion type Assertion NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_head.
- NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_assertion wasGeneratedBy ECO_0000203 NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_provenance.
- NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_assertion wasDerivedFrom befree-20150227 NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_provenance.
- NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_assertion SIO_000772 22004887 NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_provenance.
- NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_assertion evidence source_evidence_literature NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_provenance.
- NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_assertion description "[This report provide a wide spectrum of USH2A mutations and clinical features, including atypical Usher syndrome phenotypes resembling Usher syndrome type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767572.RAQWkW_XVB1n-K8loUiQJyv_MMylyghnkN-dU2dXbDRO4130_provenance.