Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_assertion> ?p ?o ?g. }
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- NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_assertion type Assertion NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_head.
- NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_assertion wasGeneratedBy ECO_0000203 NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_provenance.
- NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_assertion wasDerivedFrom befree-2016 NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_provenance.
- NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_assertion SIO_000772 9989983 NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_provenance.
- NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_assertion evidence source_evidence_literature NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_provenance.
- NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_assertion description "[SCN patients who develop secondary myelodysplastic syndrome and acute myeloid leukemia almost invariably acquired a GCSFR mutation, suggesting that this genetic alteration represents a key step in leukemogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1414862.RAptLtQCi3m14r9YKPWfVg1B9VmuNJwYcfWWJgHxprNSc130_provenance.