Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_provenance.
- NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_assertion description "[ We concluded that HSPA1B (1267)GG and HSPA1L (2437)CC genotypes were more frequent among preeclamptic than control patients, suggesting that these genotypes may play a role in the susceptibility for preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_provenance.
- NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_assertion evidence source_evidence_literature NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_provenance.
- NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_assertion SIO_000772 16202503 NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_provenance.
- NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_assertion wasDerivedFrom gad-20130706 NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_provenance.
- NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_assertion wasGeneratedBy ECO_0000203 NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_provenance.
- gad-20130706 importedOn "2013-07-06" NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_provenance.