Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_assertion> ?p ?o ?g. }
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- NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_assertion type Assertion NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_head.
- NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_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." NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_provenance.
- NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_assertion evidence source_evidence_literature NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_provenance.
- NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_assertion SIO_000772 10576500 NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_provenance.
- NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_assertion wasDerivedFrom befree-20150227 NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_provenance.
- NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_assertion wasGeneratedBy ECO_0000203 NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_provenance.