Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_assertion type Assertion NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_head.
- NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_assertion wasGeneratedBy ECO_0000203 NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_provenance.
- NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_assertion wasDerivedFrom befree-20150227 NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_provenance.
- NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_assertion SIO_000772 14594802 NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_provenance.
- NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_assertion evidence source_evidence_literature NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_provenance.
- NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_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." NP285256.RA3rAkNo2-0WYtqJKAaQU0A8-ik7kim6lqoFimuw1vBBA130_provenance.