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- NP1174997.RA97TqV3-XACc8ikSyWbP4h2dBZOgNrP0dmm0FyJBR7PI130_assertion type Assertion NP1174997.RA97TqV3-XACc8ikSyWbP4h2dBZOgNrP0dmm0FyJBR7PI130_head.
- NP1174997.RA97TqV3-XACc8ikSyWbP4h2dBZOgNrP0dmm0FyJBR7PI130_assertion wasGeneratedBy ECO_0000203 NP1174997.RA97TqV3-XACc8ikSyWbP4h2dBZOgNrP0dmm0FyJBR7PI130_provenance.
- NP1174997.RA97TqV3-XACc8ikSyWbP4h2dBZOgNrP0dmm0FyJBR7PI130_assertion wasDerivedFrom befree-2016 NP1174997.RA97TqV3-XACc8ikSyWbP4h2dBZOgNrP0dmm0FyJBR7PI130_provenance.
- NP1174997.RA97TqV3-XACc8ikSyWbP4h2dBZOgNrP0dmm0FyJBR7PI130_assertion SIO_000772 24746896 NP1174997.RA97TqV3-XACc8ikSyWbP4h2dBZOgNrP0dmm0FyJBR7PI130_provenance.
- NP1174997.RA97TqV3-XACc8ikSyWbP4h2dBZOgNrP0dmm0FyJBR7PI130_assertion evidence source_evidence_literature NP1174997.RA97TqV3-XACc8ikSyWbP4h2dBZOgNrP0dmm0FyJBR7PI130_provenance.
- NP1174997.RA97TqV3-XACc8ikSyWbP4h2dBZOgNrP0dmm0FyJBR7PI130_assertion description "[In conclusion the frequency of CSF3R mutations is highly prevalent among AML patients secondary to SCN compared to de novo AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1174997.RA97TqV3-XACc8ikSyWbP4h2dBZOgNrP0dmm0FyJBR7PI130_provenance.