Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_assertion> ?p ?o ?g. }
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- NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_assertion type Assertion NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_head.
- NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_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." NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_provenance.
- NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_assertion evidence source_evidence_literature NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_provenance.
- NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_assertion SIO_000772 25407435 NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_provenance.
- NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_assertion wasDerivedFrom befree-2016 NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_provenance.
- NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_assertion wasGeneratedBy ECO_0000203 NP1238413.RAojBckJVpRxbHVtd6qQ5rn4c7lrATr_TYeZuxmrC9GWM130_provenance.