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- source_evidence_literature type ECO_0000212 NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_provenance.
- NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_assertion description "[Using this approach, possible associations of sequence variation, and hence of variation in DNA repair, with disease risk can be assessed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_provenance.
- NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_assertion evidence source_evidence_literature NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_provenance.
- NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_assertion SIO_000772 11062157 NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_provenance.
- NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_assertion wasDerivedFrom gad-20150221 NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_provenance.
- NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_assertion wasGeneratedBy ECO_0000203 NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP81930.RAl00jqQ_BVglO_gpNyCtkTHtZeW0mGnBtdJ_Rq8liYRQ130_provenance.