Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance.
- NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_assertion description "[The rs3024409 variant allele of F13A1 was associated with 1.66-fold increased risk of VTE, while the minor alleles of HABP2 rs6585234 and rs3862019, F2R rs253061 and rs153311, and PLAUR rs344782 were each associated with lower risk of VTE (hazard ratios in the range of 0.49-0.66).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance.
- NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_assertion evidence source_evidence_literature NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance.
- NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_assertion SIO_000772 19552680 NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance.
- NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_assertion wasDerivedFrom befree-20140225 NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance.
- NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_assertion wasGeneratedBy ECO_0000203 NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance.