Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_provenance.
- NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_assertion description "[Haplotype analysis revealed that combination of certain WDR3 variants, such as haplotype CAT, increases the risk of thyroid cancer (odds ratio = 1.85, 95% confidence interval = 0.97-3.55, p = 0.063).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_provenance.
- NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_assertion evidence source_evidence_literature NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_provenance.
- NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_assertion SIO_000772 20578902 NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_provenance.
- NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_assertion wasDerivedFrom befree-20150227 NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_provenance.
- NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_assertion wasGeneratedBy ECO_0000203 NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP283230.RAHgsvvmIuxVr5IQ0hE4MJaoBFF2sNWbm0AiPsgntEfCM130_provenance.