Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_provenance.
- NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_assertion description "[This was the first study to examine the associations of the PRKCH polymorphism with GA and GC, and suggested that the AA genotype, relative to the G/G genotype, may be a higher risk genotype for severe GA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_provenance.
- NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_assertion evidence source_evidence_literature NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_provenance.
- NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_assertion SIO_000772 20602195 NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_provenance.
- NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_assertion wasDerivedFrom gad-20150221 NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_provenance.
- NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_assertion wasGeneratedBy ECO_0000203 NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP127876.RAlFnNZDWwdgZ0LzamX8QZht57kSXzmZpl0tqrSBkKZBM130_provenance.