Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_provenance.
- NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_assertion description "[With the aim to conclusively validate the strongest associations so far reported, we selected the polymorphisms rs2227667 (SERPINE1), rs17501108 (HGF), rs3136685 (CCR7), rs16944 (IL1B), rs12147254 (TRAF3), rs1805087 (MTR), rs1800629 (TNF-?), rs7516435 (CASP9), rs1042265 (BAX), rs2234922 (mEH), and rs1801133 (MTHFR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_provenance.
- NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_assertion evidence source_evidence_literature NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_provenance.
- NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_assertion SIO_000772 24521996 NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_provenance.
- NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_assertion wasDerivedFrom befree-2016 NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_provenance.
- NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_assertion wasGeneratedBy ECO_0000203 NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1154658.RA34PfhYtmUN9KgBMNlehKn10nsT2Qq0zSDnpQtp7_XtE130_provenance.