Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_provenance.
- NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_assertion description "[We hypothesize that at least two modifications of OPA1 may lead to dominant optic atrophy, that is alteration in GTPase activity and loss of the last seven C-terminal amino acids that putatively interact with other proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_provenance.
- NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_assertion evidence source_evidence_curated NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_provenance.
- NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_assertion SIO_000772 11810270 NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_provenance.
- NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_assertion wasDerivedFrom uniprot-2016 NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_provenance.
- NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_assertion wasGeneratedBy ECO_0000218 NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP1837.RAei-UeDL08MMcRARpFbbaTXR_g8lu1aKMLp7uDUVwC4I130_provenance.