Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_provenance.
- NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_assertion description "[Several other SNPs in the candidate genes, such as CTLA4, HAVCR1, and SUMO4, also had rather small p-values (<0.05), suggesting the associations between them and RA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_provenance.
- NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_assertion evidence source_evidence_literature NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_provenance.
- NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_assertion SIO_000772 18466531 NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_provenance.
- NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_assertion wasDerivedFrom gad-20150221 NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_provenance.
- NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_assertion wasGeneratedBy ECO_0000203 NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP122909.RArPRpOxtIhb8_DkEAJuChDMbZ-RWXq0Ft1Sekqm3vLSM130_provenance.