Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_provenance.
- NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_assertion wasGeneratedBy ECO_0000203 NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_provenance.
- NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_assertion wasDerivedFrom befree-20150227 NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_provenance.
- NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_assertion SIO_000772 11574150 NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_provenance.
- NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_assertion evidence source_evidence_literature NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_provenance.
- NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_assertion description "[Although the UFD1L gene has been mapped in the region commonly deleted in patients with DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), correlation between its haploinsufficiency and the phenotype has not yet been established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765883.RAlnPycSNUEqgY5ARb4LzJ0SKlNjP0VG6C20cehyXASi0130_provenance.