Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_assertion> ?p ?o ?g. }
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- NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_assertion type Assertion NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_head.
- NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_assertion description "[We focus on a newly described human immunodeficiency disorder called radiosensitivity, immunodeficiency dysmorphic features and learning difficulties (RIDDLE) syndrome, with particular reference to the function of the defective gene, RNF168.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.
- NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_assertion evidence source_evidence_literature NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.
- NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_assertion SIO_000772 21426255 NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.
- NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_assertion wasDerivedFrom befree-2016 NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.
- NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_assertion wasGeneratedBy ECO_0000203 NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.