Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.
- befree-2016 importedOn "2016-02-19" NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.
- NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_assertion wasGeneratedBy ECO_0000203 NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.
- NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_assertion wasDerivedFrom befree-2016 NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.
- NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_assertion SIO_000772 10024240 NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.
- NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_assertion evidence source_evidence_literature NP245868.RAOw4C1-1PTJAwptBbCET8RlpITuH4E0qDJlVuzKOaDvM130_provenance.
- 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.