Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_provenance.
- NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_assertion description "[The variant AGT Thr235 allele was more common in patients without a family history of cardiovascular disease than in patients with this risk factor (p?<?0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_provenance.
- NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_assertion evidence source_evidence_literature NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_provenance.
- NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_assertion SIO_000772 21657802 NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_provenance.
- NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_assertion wasDerivedFrom befree-20150227 NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_provenance.
- NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_assertion wasGeneratedBy ECO_0000203 NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP228960.RA5H416kYvv06WFHZ0ONB-kqeJrXfN6tSqqCVD-4laTFM130_provenance.