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- source_evidence_literature type ECO_0000212 NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_provenance.
- NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_assertion description "[Among the polymorphisms genotyped, we identified eight genes (CNTNAP2, LEPR, CRHR1, NTAN1, SLC12A3, ALPL, BGLAP, and APOB) containing variants that were associated with hypertension (chi2 P values 0.002-0.048), several of which interact with the hypothalamus-pituitary-adrenal axis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_provenance.
- NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_assertion evidence source_evidence_literature NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_provenance.
- NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_assertion SIO_000772 18496130 NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_provenance.
- NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_assertion wasDerivedFrom befree-2016 NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_provenance.
- NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_assertion wasGeneratedBy ECO_0000203 NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP672289.RA3Xuhn8e6o0aamh0QsE0a8XlOWpcA1k-Hgi2cLBu4lXQ130_provenance.