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- source_evidence_literature type ECO_0000212 NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_provenance.
- NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_assertion description "[Forty Caucasian female participants meeting the Research Diagnostic Criteria for TMD were genotyped for COMT polymorphisms and completed a randomized, double-blind, placebo-controlled, two-period crossover pilot study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_provenance.
- NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_assertion evidence source_evidence_literature NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_provenance.
- NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_assertion SIO_000772 20216107 NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_provenance.
- NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_assertion wasDerivedFrom befree-20150227 NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_provenance.
- NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_assertion wasGeneratedBy ECO_0000203 NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP322213.RAe-JJ_HIFnjPK4YjE6GCeEMGNWUa2pgf1edDH-Cr5auM130_provenance.