Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_provenance.
- NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_assertion description "[study in European patients with CHD and CVD did not show any association between SNP +2255 in VKORC1 and cardiovascular disease, as opposed to findings in a Chinese population and a French study in patients with venous thromboembolism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_provenance.
- NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_assertion evidence source_evidence_literature NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_provenance.
- NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_assertion SIO_000772 18826394 NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_provenance.
- NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_assertion wasDerivedFrom lhgdn-20090331 NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_provenance.
- NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_assertion wasGeneratedBy ECO_0000203 NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP123785.RAajlBY5776Fni7rzEw-4Kh8g0pUWQxLOWlst6kR87jd4130_provenance.