Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_provenance.
- NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_assertion description "[The proposed risk-associated genotypes are NAT2 slow acetylator (without wild-type NAT2*4 allele), CYP2E1 *1A/*1A (homozygous wild type) and homozygous null GSTM1 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_provenance.
- NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_assertion evidence source_evidence_literature NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_provenance.
- NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_assertion SIO_000772 17269890 NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_provenance.
- NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_assertion wasDerivedFrom befree-2016 NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_provenance.
- NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_assertion wasGeneratedBy ECO_0000203 NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_provenance.
- befree-2016 importedOn "2016-02-19" NP591814.RAMVTl3q3lWECLLhmk0V1M2Z4aVMhOUaqf3h6Glf0c1P0130_provenance.