Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_provenance.
- NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_assertion description "[After haplotype reconstruction, logistic regression analyses adjusted for traditional risk factors and COPD showed a significant association among AAA and AHCY, FOLH1, MTHFD1, MTR, NNMT, PON1 and TYMS haplotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_provenance.
- NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_assertion evidence source_evidence_literature NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_provenance.
- NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_assertion SIO_000772 18635682 NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_provenance.
- NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_assertion wasDerivedFrom gad-20150221 NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_provenance.
- NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_assertion wasGeneratedBy ECO_0000203 NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP125827.RAAgONW8DWAwX4dWXVRSLLMW92on0cetxCU3r2Zz8rDoM130_provenance.