Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP419012.RA66DI2JHhNIBWrOzTZ9EZs5zvSvczr2y86wc3IWN2v30130_provenance.