Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_assertion type Assertion NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_head.
- NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_assertion description "[Two hereditary human leukemia syndromes are severe congenital neutropenia (SCN), caused by mutations in the gene ELA2, encoding the protease neutrophil elastase, and familial platelet disorder with acute myelogenous leukemia (AML), caused by mutations in the gene AML1, encoding the transcription factor core-binding factor alpha (CBFalpha).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_provenance.
- NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_assertion evidence source_evidence_literature NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_provenance.
- NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_assertion SIO_000772 14594802 NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_provenance.
- NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_assertion wasDerivedFrom befree-20140225 NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_provenance.
- NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_assertion wasGeneratedBy ECO_0000203 NP423440.RAWdq8zW3dB5-GEVdC3mXPPz_8JtDJpuQ2ArkphSjJ1CQ130_provenance.