Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_assertion> ?p ?o ?g. }
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- NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_assertion type Assertion NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_head.
- NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_assertion wasGeneratedBy ECO_0000203 NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_provenance.
- NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_assertion wasDerivedFrom befree-2016 NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_provenance.
- NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_assertion SIO_000772 24746896 NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_provenance.
- NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_assertion evidence source_evidence_literature NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_provenance.
- NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_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." NP1174999.RA_CWzIFw2U6XEzNU2EbcuI_9oj_GA4xsqu9tm2yz5B9Y130_provenance.