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- source_evidence_literature type ECO_0000212 NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_provenance.
- NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_assertion description "[A haplotype encompassing the variant allele of DNA repair gene polymorphism ERCC2/XPD Lys751Gln but not the variant allele of Asp312Asn is associated with risk of lung cancer in a northeastern Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_provenance.
- NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_assertion evidence source_evidence_literature NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_provenance.
- NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_assertion SIO_000772 17498557 NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_provenance.
- NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_assertion wasDerivedFrom befree-2016 NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_provenance.
- NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_assertion wasGeneratedBy ECO_0000203 NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_provenance.
- befree-2016 importedOn "2016-02-19" NP609643.RAWEAl0aJmhExMnFhVQBtzCo_Wh23Dl9CMIKX8AEo37aA130_provenance.