Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_provenance.
- NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_assertion description "[These genetic changes include haploinsufficiency of SETBP1 associated with intellectual disability and loss of expressive language and truncations of ZMYND11 in individuals with autism, aggression and complex neuropsychiatric features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_provenance.
- NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_assertion evidence source_evidence_curated NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_provenance.
- NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_assertion SIO_000772 25217958 NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_provenance.
- NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_assertion wasDerivedFrom ctd_human-20150221 NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_provenance.
- NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_assertion wasGeneratedBy ECO_0000218 NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP29545.RAIy4Yb0VQ3-CZHtDc1OeVoK2RMVL5dkbb2FBS5RlPYuw130_provenance.