Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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." provenance.
- 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." provenance.
- NP440459.RARCMeIXTpzbWlca7W9V8O8nxeZt7vId1j9-MPRKFwT0A130_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." NP440459.RARCMeIXTpzbWlca7W9V8O8nxeZt7vId1j9-MPRKFwT0A130_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.
- NP268530.RAVbGqBqCPxMF7sI1DoUxcpbwlQcOjH0L14AZWR96e6mA130_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." NP268530.RAVbGqBqCPxMF7sI1DoUxcpbwlQcOjH0L14AZWR96e6mA130_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.