Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_assertion type Assertion NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_head.
- NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_assertion description "[Inherited or sporadic heterozygous mutations in the transcription factor GATA2 lead to a clinical syndrome characterized by non-tuberculous mycobacterial and other opportunistic infections, a severe deficiency in monocytes, B cells and natural killer cells, and progression from a hypocellular myelodysplastic syndrome to myeloid leukemias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_provenance.
- NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_assertion evidence source_evidence_literature NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_provenance.
- NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_assertion SIO_000772 24077845 NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_provenance.
- NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_assertion wasDerivedFrom befree-20150227 NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_provenance.
- NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_assertion wasGeneratedBy ECO_0000203 NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_provenance.