Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_provenance.
- NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_assertion description "[Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_provenance.
- NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_assertion evidence source_evidence_curated NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_provenance.
- NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_assertion SIO_000772 24566826 NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_provenance.
- NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_assertion wasDerivedFrom uniprot-2016 NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_provenance.
- NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_assertion wasGeneratedBy ECO_0000218 NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7808.RAcbiVpRI3XCt4fMhTCNa46j9-ah2ow63nWYRK-6813YM130_provenance.