Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_provenance.
- NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_assertion description "[Heterozygote carriers of SNPs in CYP1A2 1545T>C, -164C>A and -740T>G; CYP2A6 -47A>C; MDR1 3435T>C; NAT1 1088T>A and 1095A>C; GSTA2 S112T; GSTM3 V224I and MTHFR A222V had altered risk of developing lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_provenance.
- NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_assertion evidence source_evidence_literature NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_provenance.
- NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_assertion SIO_000772 17259654 NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_provenance.
- NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_assertion wasDerivedFrom gad-20150221 NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_provenance.
- NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_assertion wasGeneratedBy ECO_0000203 NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_provenance.
- gad-20150221 importedOn "2015-02-21" NP81884.RAxLDrX66v3Cc0nUC-b_FrnaWSnc5Q3GcJ-3xG0ouhnig130_provenance.