Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_provenance.
- NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_assertion description "[Random-effects meta-analyses of 81 eligible polymorphisms evaluated in >4 data sets confirmed 20 single-nucleotide polymorphisms across 10 loci (TYR, AFG3L1P, CDK10, MYH7B, SLC45A2, MTAP, ATM, CLPTM1L, FTO, and CASP8) that have previously been published with genome-wide significant evidence for association (P<5 � 10(-8)) with CM risk, with certain variants possibly functioning as proxies of already tagged genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_provenance.
- NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_assertion evidence source_evidence_literature NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_provenance.
- NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_assertion SIO_000772 25407435 NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_provenance.
- NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_assertion wasDerivedFrom befree-2016 NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_provenance.
- NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_assertion wasGeneratedBy ECO_0000203 NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1238411.RAQK-EqtNydyywrqdJkA9dzEzs_cGkjDnWndkDoX9HsTk130_provenance.