Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_provenance.
- NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_assertion description "[These results show that GSTM1 null genotype may play a significant role in the aetiopathogeneses of DM and the GSTM1 gene may be a useful marker in the prediction of DM susceptibility of the Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_provenance.
- NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_assertion evidence source_evidence_literature NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_provenance.
- NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_assertion SIO_000772 16927413 NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_provenance.
- NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_assertion wasDerivedFrom gad-20130706 NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_provenance.
- NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_assertion wasGeneratedBy ECO_0000203 NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP87525.RA10N-yFQtJDawk-bsRHrbrk_feI_bcZpga4BZ4QLZkLk130_provenance.