Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_provenance.
- NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_assertion description "[This function is compromised by two CDAI mutations that impair complex formation with Asf1, providing insight into the molecular basis for CDAI disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_provenance.
- NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_assertion evidence source_evidence_curated NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_provenance.
- NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_assertion SIO_000772 22407294 NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_provenance.
- NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_assertion wasDerivedFrom uniprot-2016 NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_provenance.
- NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_assertion wasGeneratedBy ECO_0000218 NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6998.RAdMgbQYM9aotRxjCNQ1IqBOITmZPYAqM7pmDRLeI9Lrk130_provenance.