Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_provenance.
- NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_assertion description "[The role of inherited prothrombotic conditions, including factor V Leiden (FV G1691A), prothrombin G20210A, and the methylenetetrahydrofolate reductase (MTHFR) C677T genotype, in the pathogenesis of ischemic stroke is not well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_provenance.
- NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_assertion evidence source_evidence_literature NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_provenance.
- NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_assertion SIO_000772 15946211 NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_provenance.
- NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_assertion wasDerivedFrom befree-20140225 NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_provenance.
- NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_assertion wasGeneratedBy ECO_0000203 NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_provenance.
- befree-20140225 importedOn "2014-02-25" NP177647.RA5kBwX5HGOfCt2MB2_Gqmak6oLp2dsYYfWWhbN8Gghws130_provenance.