Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_provenance.
- NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_assertion description "[The IL-10-592 SNP CA (P=0.0012/OR=2.4/CI:1.4-4.1), AA (P=0.0458/OR=2.3/CI:1.1-4.9), and CA+AA (P=0.0006/OR=2.4/CI:1.4-3.4) genotypes and the allele A (P=0.0036/OR=1.7/CI:1.2-2.4) were found to be significantly more prevalent in the CP group when compared with control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_provenance.
- NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_assertion evidence source_evidence_literature NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_provenance.
- NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_assertion SIO_000772 18725394 NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_provenance.
- NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_assertion wasDerivedFrom befree-20140225 NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_provenance.
- NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_assertion wasGeneratedBy ECO_0000203 NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP189176.RA-_7HD8BJ9v_2CMIAZA86mAy-MywHa9OrBnGIRVFllyo130_provenance.