Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_assertion type Assertion NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_head.
- NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_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." NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.
- NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_assertion evidence source_evidence_literature NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.
- NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_assertion SIO_000772 10024240 NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.
- NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_assertion wasDerivedFrom befree-2016 NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.
- NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_assertion wasGeneratedBy ECO_0000203 NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.