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- source_evidence_literature type ECO_0000212 NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_provenance.
- NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_assertion description "[There was a significant association of FAAH genotype with FGID phenotype (overall chi(2), P = 0.011) and with specific individual phenotypes (P = 0.048).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_provenance.
- NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_assertion evidence source_evidence_literature NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_provenance.
- NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_assertion SIO_000772 17962356 NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_provenance.
- NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_assertion wasDerivedFrom befree-2016 NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_provenance.
- NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_assertion wasGeneratedBy ECO_0000203 NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_provenance.
- befree-2016 importedOn "2016-02-19" NP637251.RAymElIrLnZwy4EuHBxyQBsRc5Uk3N6UEm5_j3ru5G_kY130_provenance.