Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_assertion> ?p ?o ?g. }
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- NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_assertion type Assertion NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_head.
- NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_assertion description "[The human UFD1L gene was deleted in all 182 patients studied with 22q11 deletion, and a smaller deletion of approximately 20 kilobases that removed exons 1 to 3 of UFD1L was found in one individual with features typical of 22q11 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_provenance.
- NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_assertion evidence source_evidence_literature NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_provenance.
- NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_assertion SIO_000772 10024240 NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_provenance.
- NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_assertion wasDerivedFrom befree-20150227 NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_provenance.
- NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_assertion wasGeneratedBy ECO_0000203 NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_provenance.