Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_provenance.
- NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_assertion description "[Resequencing of NTF4 revealed a nonsynonymous (A88V), silent (P151P) and two changes in the 3'UTR region, along with a known polymorphism (rs11669977) in cases of POAG; the PACG cases exhibited only the A88V variation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_provenance.
- NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_assertion evidence source_evidence_literature NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_provenance.
- NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_assertion SIO_000772 20463313 NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_provenance.
- NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_assertion wasDerivedFrom befree-20150227 NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_provenance.
- NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_assertion wasGeneratedBy ECO_0000203 NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP599631.RATnq8U5aJK3dusdUkXQmsXWM2bfWtuGZYjDihraPUeHM130_provenance.