Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_provenance.
- NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_assertion description "[However, fixed-effects model showed significant risk of AML in the presence of null genotypes of GSTM1 and GSTT1(p < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_provenance.
- NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_assertion evidence source_evidence_literature NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_provenance.
- NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_assertion SIO_000772 19811334 NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_provenance.
- NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_assertion wasDerivedFrom befree-20150227 NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_provenance.
- NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_assertion wasGeneratedBy ECO_0000203 NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP437709.RAbhvbTElwHbJ5RXx_aL5xz7TluzlSGfC1kvLVZ3-VLMA130_provenance.