Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_provenance.
- NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_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." NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_provenance.
- NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_assertion evidence source_evidence_literature NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_provenance.
- NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_assertion SIO_000772 18496130 NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_provenance.
- NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_assertion wasDerivedFrom befree-20140225 NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_provenance.
- NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_assertion wasGeneratedBy ECO_0000203 NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP819838.RATH0q7QyOlFvVtiLOiwQgSSwx59GNHGBBpGswyxlyZyE130_provenance.