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- source_evidence_literature type ECO_0000212 NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_provenance.
- NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_assertion description "[Common variant alleles at the XPD (312Asn, 751Gln) and XRCC1 (399Gln) loci have been identified and associated with increased risk for lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_provenance.
- NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_assertion evidence source_evidence_literature NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_provenance.
- NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_assertion SIO_000772 12552590 NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_provenance.
- NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_assertion wasDerivedFrom befree-2016 NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_provenance.
- NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_assertion wasGeneratedBy ECO_0000203 NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_provenance.
- befree-2016 importedOn "2016-02-19" NP381729.RAhW7XoUp-1k6FTJ8CL-h8wB1xG6OG4hwZ9BhbgcAOQ3w130_provenance.