Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_provenance.
- NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_assertion description "[In white CHS participants, the prespecified risk alleles of 7 of the 74 SNPs (in HPS1, ITGAE, ABCG2, MYH15, FSTL4, CALM1, and BAT2) were nominally associated with increased risk of stroke (one-sided P<0.05, false discovery rate=0.42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_provenance.
- NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_assertion evidence source_evidence_literature NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_provenance.
- NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_assertion SIO_000772 19023099 NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_provenance.
- NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_assertion wasDerivedFrom gad-20150221 NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_provenance.
- NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_assertion wasGeneratedBy ECO_0000203 NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP97519.RARdOa9giI3JWftZsrEsxemzwQVm1WCmyh937WKmqp0Vk130_provenance.