Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_provenance.
- NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_assertion description "[Seven novel mutations of the ADAR gene in Chinese families and sporadic patients with dyschromatosis symmetrica hereditaria (DSH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_provenance.
- NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_assertion evidence source_evidence_curated NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_provenance.
- NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_assertion SIO_000772 15146470 NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_provenance.
- NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_assertion wasDerivedFrom uniprot-20130724 NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_provenance.
- NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_assertion wasGeneratedBy ECO_0000218 NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP214.RAS6OHj6K8vJXFWHryYJTBCiXgguDsxZeDEh53akSApfU130_provenance.