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- source_evidence_literature type ECO_0000212 NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP765899.RACv7soMBTodjRGtxNoTIkMXG4ER1C57higbN5cH1XGKA130_provenance.