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- source_evidence_literature type ECO_0000212 NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_provenance.
- NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_assertion description "[These results suggest that the GSTT1 null genotype may play a role in an increased risk of myelodysplasia unrelated to other mechanisms of myelodysplasia, such as chromosomal alterations or mutation of TP53 or NRAS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_provenance.
- NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_assertion evidence source_evidence_literature NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_provenance.
- NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_assertion SIO_000772 10576500 NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_provenance.
- NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_assertion wasDerivedFrom befree-2016 NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_provenance.
- NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_assertion wasGeneratedBy ECO_0000203 NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_provenance.
- befree-2016 importedOn "2016-02-19" NP268536.RADSRktQmSBoN25z5l91Dalv-KHsOmeDeS_EXgBSyefmk130_provenance.