Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_provenance.
- NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_assertion description "[This paper provides a concise review of the 24 published studies that evaluated the risk of SCCHN in relation to two deletion polymorphisms of the glutathione S-transferase family: GSTM1 and GSTT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_provenance.
- NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_assertion evidence source_evidence_literature NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_provenance.
- NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_assertion SIO_000772 11447041 NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_provenance.
- NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_assertion wasDerivedFrom befree-2016 NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_provenance.
- NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_assertion wasGeneratedBy ECO_0000203 NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_provenance.
- befree-2016 importedOn "2016-02-19" NP323524.RAE8Qc1y4ts2csUBetcqbJ2n4ynVFXB8Zv_kjAuLPc0n0130_provenance.