Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1413069.RAKRte4RAXaoNFgqsl33qtoRZ7k69J1T6vEYrVpSSF-jQ#assertion> ?p ?o ?g. }
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- assertion description "[While recessive mutations in RNF168 cause RIDDLE syndrome, an immune deficiency and radiosensitivity disorder, the potential impact of heterozygous deletion of RNF168 on patients with the 3q29 deletion syndrome is still unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 21626679 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.