Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_assertion> ?p ?o ?g. }
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- NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_assertion type Assertion NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_head.
- NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_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." NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_provenance.
- NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_assertion evidence source_evidence_literature NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_provenance.
- NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_assertion SIO_000772 14594802 NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_provenance.
- NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_assertion wasDerivedFrom befree-20140225 NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_provenance.
- NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_assertion wasGeneratedBy ECO_0000203 NP716478.RAByKMAbEMy46qD8TYg4gS4YoS80nU6NwQ98-ryiwxCgo130_provenance.