Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_provenance.
- NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_assertion description "[The G allele and the (-116 G/G) genotype of the XBP1 (-116 C/G) gene polymorphism were found to be a significant risk factor for the patients with Ischemic Stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_provenance.
- NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_assertion evidence source_evidence_literature NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_provenance.
- NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_assertion SIO_000772 19669932 NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_provenance.
- NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_assertion wasDerivedFrom befree-20140225 NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_provenance.
- NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_assertion wasGeneratedBy ECO_0000203 NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP881441.RA7hdnX94oQNj1qEHHWfqiBDnhxyjw05o-VT4fizHC4x8130_provenance.