Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_provenance.
- NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_assertion description "[De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_provenance.
- NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_assertion evidence source_evidence_curated NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_provenance.
- NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_assertion SIO_000772 25326669 NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_provenance.
- NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_assertion wasDerivedFrom uniprot-2016 NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_provenance.
- NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_assertion wasGeneratedBy ECO_0000218 NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8037.RActOhrOe8ee3OvEBEreFBK_C1W7SrmBcwdaoTtFKbpn8130_provenance.