Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_assertion> ?p ?o ?g. }
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- NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_assertion type Assertion NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_head.
- NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_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." NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_provenance.
- NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_assertion evidence source_evidence_literature NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_provenance.
- NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_assertion SIO_000772 21626679 NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_provenance.
- NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_assertion wasDerivedFrom befree-20150227 NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_provenance.
- NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_assertion wasGeneratedBy ECO_0000203 NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_provenance.