Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_provenance.
- NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_assertion description "[Metaanalysis of the weighted 6-SNP score, on the basis of polymorphisms in CELSR2 (cadherin, EGF LAG 7-pass G-type receptor 2), APOB (apolipoprotein B), ABCG5/8 [ATP-binding cassette, sub-family G (WHITE), member 5/8], LDLR (low density lipoprotein receptor), and APOE (apolipoprotein E) loci, in the independent FH/M- cohorts showed a consistently higher score in comparison to the WHII population (P < 2.2 � 10(-16)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_provenance.
- NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_assertion evidence source_evidence_literature NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_provenance.
- NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_assertion SIO_000772 25414277 NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_provenance.
- NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_assertion wasDerivedFrom befree-2016 NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_provenance.
- NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_assertion wasGeneratedBy ECO_0000203 NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1239049.RAD1fknv6ybCu5QrmK0Ajf7ngvY4gaCsi1wauOES07Ru4130_provenance.