Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_assertion> ?p ?o ?g. }
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- NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_assertion type Assertion NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_head.
- NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_assertion description "[Mutations in CSF3R are common in patients with CNL or atypical CML and represent a potentially useful criterion for diagnosing these neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_provenance.
- NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_assertion evidence source_evidence_literature NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_provenance.
- NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_assertion SIO_000772 23656643 NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_provenance.
- NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_assertion wasDerivedFrom befree-20140225 NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_provenance.
- NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_assertion wasGeneratedBy ECO_0000203 NP408769.RAHxeX9RdlgS4YmbobE-Wm5T6Y6rhtOOn8l3-DTOnWHtM130_provenance.