Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP328713.RAq5PIQvXxPUB1V_Vug-xsnfFnnoidEfRZn5jCC7vwLdE130_provenance.