Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_assertion> ?p ?o ?g. }
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- NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_assertion type Assertion NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_head.
- NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_assertion description "[High frequency of NAD(P)H:quinone oxidoreductase 1 (NQO1) C(609)T germline polymorphism in MDS/AML with trisomy 8.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_provenance.
- NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_assertion evidence source_evidence_literature NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_provenance.
- NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_assertion SIO_000772 23643325 NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_provenance.
- NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_assertion wasDerivedFrom befree-20150227 NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_provenance.
- NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_assertion wasGeneratedBy ECO_0000203 NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_provenance.