Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_provenance.
- NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_assertion description "[We found that the haplotype CT of IL1B -31 and +3954 polymorphisms showed higher association with risk to chagasic cardiomyopathy (p(c) = 0.008, OR = 12.53) and the extended haplotype (CCTCATT) was significantly more frequent in asymptomatic than in cardiomyopathic patients (p = 0.0014, p(c) = 0.011, OR = 0.17).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_provenance.
- NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_assertion evidence source_evidence_literature NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_provenance.
- NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_assertion SIO_000772 17002905 NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_provenance.
- NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_assertion wasDerivedFrom befree-20150227 NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_provenance.
- NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_assertion wasGeneratedBy ECO_0000203 NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP490491.RAFg6N0A621do_czc0tykLMwoEJM4Umnzi6d4355R2Sfc130_provenance.