Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_provenance.
- NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_assertion description "[Conclusion: Data of this study indicate that neonates and infants with underlying cardiac disease and basically increased PAI-1 due to the 4G/4G variant of the PAI-1 promoter polymorphism along with elevated t-PA levels in combination with further prothrombotic risk factors are at high risk of developing early thromboembolism during cardiac catheterisation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_provenance.
- NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_assertion evidence source_evidence_literature NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_provenance.
- NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_assertion SIO_000772 11457466 NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_provenance.
- NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_assertion wasDerivedFrom befree-20140225 NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_provenance.
- NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_assertion wasGeneratedBy ECO_0000203 NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP642874.RAmFcE_HtEc2CLmVpQHl5hiHlMYP4cu-gm61FMeAv-mnU130_provenance.