Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_assertion> ?p ?o ?g. }
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- NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_assertion type Assertion NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_head.
- NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_assertion wasGeneratedBy ECO_0000203 NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_provenance.
- NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_assertion wasDerivedFrom befree-2016 NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_provenance.
- NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_assertion SIO_000772 22004887 NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_provenance.
- NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_assertion evidence source_evidence_literature NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_provenance.
- NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_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." NP931598.RABfPZmpFqrEWz7Z2AVa_UQ0YhHsZJso2VfGlBXludgGk130_provenance.