Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_provenance.
- NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_assertion description "[When ten CHARGE SNPs for each trait were included in a joint meta-analysis with the Global BPgen Consortium (n = 34,433), four CHARGE loci attained genome-wide significance (P < 5 A 10(-8)) for SBP (ATP2B1, CYP17A1, PLEKHA7, SH2B3), six for DBP (ATP2B1, CACNB2, CSK-ULK3, SH2B3, TBX3-TBX5, ULK4) and one for hypertension (ATP2B1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_provenance.
- NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_assertion evidence source_evidence_literature NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_provenance.
- NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_assertion SIO_000772 19430479 NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_provenance.
- NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_assertion wasDerivedFrom gad-20150221 NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_provenance.
- NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_assertion wasGeneratedBy ECO_0000203 NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP123406.RARyUTHuERRBE-kDjOMgnkAK6KubW3uG7f7kPYrYBI4BM130_provenance.