Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP977633.RAiWGhwML3JkYEVc8jt8YHbXxyLQWSlX-YVdFoDnvRbMQ130_provenance.