Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_assertion> ?p ?o ?g. }
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- NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_assertion type Assertion NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_head.
- NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_assertion description "[Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_provenance.
- NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_assertion evidence source_evidence_curated NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_provenance.
- NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_assertion SIO_000772 16648378 NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_provenance.
- NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_assertion wasDerivedFrom uniprot-2016 NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_provenance.
- NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_assertion wasGeneratedBy ECO_0000218 NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_provenance.