Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP440524.RAJdsFmnS6N7MM6PjvHcJyD3cZKgz-XDCXKxcG18-TZqk130_provenance.