Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_provenance.
- NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_assertion description "[Combination of NAT2 fast acetylator and GSTM1 null genotype posed a significantly increased risk of MM in the Italian, but not in the Finnish study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_provenance.
- NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_assertion evidence source_evidence_literature NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_provenance.
- NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_assertion SIO_000772 16697254 NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_provenance.
- NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_assertion wasDerivedFrom befree-2016 NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_provenance.
- NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_assertion wasGeneratedBy ECO_0000203 NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_provenance.
- befree-2016 importedOn "2016-02-19" NP549481.RA3xKg_t9nbCLGXcY5FYl6a67LQrWuSp1UvLO5HCF6Q_E130_provenance.