Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_provenance.
- NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_assertion description "[These findings suggest that the 20210A prothrombin allele represents an inherited risk factor for acute coronary syndrome among patients who have limited extent of coronary disease at angiography or who lack major metabolic and acquired risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_provenance.
- NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_assertion evidence source_evidence_literature NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_provenance.
- NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_assertion SIO_000772 11741359 NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_provenance.
- NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_assertion wasDerivedFrom befree-20140225 NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_provenance.
- NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_assertion wasGeneratedBy ECO_0000203 NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP198765.RAxco27x8CajX2rY_jwD5c-o57RDIWdXzeqsS_FshoyaQ130_provenance.