Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_provenance.
- NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_assertion description "[Due to the controversial results about the role of the ATR1 gene locus in hypertension and understanding that ethnic origin should be carefully considered in studying the association between gene polymorphism and disease etiology, we investigated the role of A1166C polymorphism in Serbian hypertensives.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_provenance.
- NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_assertion evidence source_evidence_literature NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_provenance.
- NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_assertion SIO_000772 12482634 NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_provenance.
- NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_assertion wasDerivedFrom befree-20140225 NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_provenance.
- NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_assertion wasGeneratedBy ECO_0000203 NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP487915.RAXxbs2YSJ3yHbbtXhFsdx0OHn6W9DvKX09_a6kmEbY0A130_provenance.