Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_provenance.
- NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_assertion wasGeneratedBy ECO_0000203 NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_provenance.
- NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_assertion wasDerivedFrom befree-2016 NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_provenance.
- NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_assertion SIO_000772 22952149 NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_provenance.
- NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_assertion evidence source_evidence_literature NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_provenance.
- NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_assertion description "[Moreover, simultaneous carriage of both, the GSTM1 and the GSTT1 null genotypes, was almost identical in both groups (10.7% in GC vs. 10.6% in HC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010613.RAx3wAhZso9eke9rx7Q6T-7Mi2BLV8QHXwXBkbf0NGyD4130_provenance.