Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_provenance.
- NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_assertion description "[Genetic variations in the tissue factor gene are associated with clinical outcome in acute coronary syndrome and expression levels in human monocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_provenance.
- NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_assertion evidence source_evidence_literature NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_provenance.
- NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_assertion SIO_000772 16239598 NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_provenance.
- NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_assertion wasDerivedFrom befree-20150227 NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_provenance.
- NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_assertion wasGeneratedBy ECO_0000203 NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_provenance.
- befree-20150227 importedOn "2015-02-27" NP391130.RAvMsaw88_IbI52dwO2VvlGk1VT6X8NorE7CQ3BY9R9Ag130_provenance.