Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_provenance.
- NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_assertion wasGeneratedBy ECO_0000203 NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_provenance.
- NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_assertion wasDerivedFrom gad-20150221 NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_provenance.
- NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_assertion SIO_000772 15248218 NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_provenance.
- NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_assertion evidence source_evidence_literature NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_provenance.
- NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_assertion description "[Patients who were either heterozygous or homozygous for CYP2C19*2 had a significantly lower risk of developing premature ovarian failure (relative risk 0.10; 95% confidence interval 0.02-0.52), after adjustment for age and total number of cyclophosphamide pulses received.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86701.RA_DEJ3b0lJ01IeTRt5FG1bBFUbGrlR8w5DiQlBSDnWxs130_provenance.