Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_provenance.
- NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_assertion description "[The frequency of subject with the homozygote of 12 repeat allele was significantly higher in patients with hypertension compared with control subjects (987 cases, 924 controls) (P=0.030; odds ratio=1.24) at a novel VNTR polymorphism of CIAS1 intron 4 loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_provenance.
- NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_assertion evidence source_evidence_literature NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_provenance.
- NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_assertion SIO_000772 16868559 NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_provenance.
- NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_assertion wasDerivedFrom befree-20150227 NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_provenance.
- NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_assertion wasGeneratedBy ECO_0000203 NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_provenance.