Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_provenance.
- 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.
- uniprot-2016 importedOn "2016-01-25" NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_provenance.