Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_provenance.
- NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_assertion description "[Furthermore, a strong association was observed between the combination of GSTT1 null and GSTM1 null genotype and risk of BC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_provenance.
- NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_assertion evidence source_evidence_literature NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_provenance.
- NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_assertion SIO_000772 22339266 NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_provenance.
- NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_assertion wasDerivedFrom befree-2016 NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_provenance.
- NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_assertion wasGeneratedBy ECO_0000203 NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_provenance.
- befree-2016 importedOn "2016-02-19" NP961232.RAQ3Xe_P1IU0_Zh1CQd00lA758CKwtkxR8SBAS9mM1BlE130_provenance.