Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_provenance.
- NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_assertion description "[The study also shows that carriers of the A3 haplotype have a reduced risk of myocardial infarction, only in part due to increased soluble endothelial protein C levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_provenance.
- NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_assertion evidence source_evidence_literature NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_provenance.
- NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_assertion SIO_000772 18757851 NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_provenance.
- NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_assertion wasDerivedFrom befree-20140225 NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_provenance.
- NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_assertion wasGeneratedBy ECO_0000203 NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP807187.RAmFgUnmty310RyWxeK0eVTWbBUqFJ5maM_jHQfyG-VX8130_provenance.