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- source_evidence_literature type ECO_0000212 NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_provenance.
- NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_assertion description "[A study of 222 candidate genes in type 2 diabetes reported association of variants in RAPGEF1, ENPP1, TP53, NRF1, SLC2A2, SLC2A4 and FOXC2 with type 2 diabetes in 4,805 Finnish individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_provenance.
- NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_assertion evidence source_evidence_literature NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_provenance.
- NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_assertion SIO_000772 21283750 NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_provenance.
- NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_assertion wasDerivedFrom befree-2016 NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_provenance.
- NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_assertion wasGeneratedBy ECO_0000203 NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_provenance.
- befree-2016 importedOn "2016-02-19" NP869262.RAhy_ZqL17xBeW9gCG0ySGZEVW4YFJxnNLwbgQi9DcZlU130_provenance.