Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_provenance.
- NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_assertion description "[The risk of hypertension was significantly increased in the GSTA1*B allele carriers having also the GSTM1 null genotype or both the GSTM1 and GSTT1 null genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_provenance.
- NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_assertion evidence source_evidence_literature NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_provenance.
- NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_assertion SIO_000772 18300949 NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_provenance.
- NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_assertion wasDerivedFrom lhgdn-20090331 NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_provenance.
- NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_assertion wasGeneratedBy ECO_0000203 NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP234878.RACJWH0H8HvyCNCDvjNUFH_vB6asEbG4IkIwyh1qHUddQ130_provenance.