Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_provenance.
- NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_assertion wasGeneratedBy ECO_0000203 NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_provenance.
- NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_assertion wasDerivedFrom gad-20150221 NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_provenance.
- NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_assertion SIO_000772 17687452 NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_provenance.
- NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_assertion evidence source_evidence_literature NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_provenance.
- NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_assertion description "[For XPD, having variation at both loci (312Asn and 751Gln) occurred less frequently among BCC and SCC cases compared with controls (OR = 0.8; 95% CI, 0.6-1.0) for both case groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141390.RA4uS9Vc_j6H1tMmsxBgv9nFfZhD1In0JwCOvYXs5SeyI130_provenance.