Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance.
- NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_assertion description "[The present meta-analysis demonstrated that the GSTM1 and GSTT1 null genotype may be associated with an increased risk of HCC and that individuals having the combination of both defective GST genotypes may be more susceptible to developing HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance.
- NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_assertion evidence source_evidence_literature NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance.
- NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_assertion SIO_000772 24399650 NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance.
- NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_assertion wasDerivedFrom befree-20150227 NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance.
- NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_assertion wasGeneratedBy ECO_0000203 NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance.