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- NP418957.RAa68LS0yuBcoUNQ1N-gCp6WSFJgT3ujxgAnXR9cOHhc4130_assertion type Assertion NP418957.RAa68LS0yuBcoUNQ1N-gCp6WSFJgT3ujxgAnXR9cOHhc4130_head.
- NP418957.RAa68LS0yuBcoUNQ1N-gCp6WSFJgT3ujxgAnXR9cOHhc4130_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." NP418957.RAa68LS0yuBcoUNQ1N-gCp6WSFJgT3ujxgAnXR9cOHhc4130_provenance.
- NP418957.RAa68LS0yuBcoUNQ1N-gCp6WSFJgT3ujxgAnXR9cOHhc4130_assertion evidence source_evidence_literature NP418957.RAa68LS0yuBcoUNQ1N-gCp6WSFJgT3ujxgAnXR9cOHhc4130_provenance.
- NP418957.RAa68LS0yuBcoUNQ1N-gCp6WSFJgT3ujxgAnXR9cOHhc4130_assertion SIO_000772 14594802 NP418957.RAa68LS0yuBcoUNQ1N-gCp6WSFJgT3ujxgAnXR9cOHhc4130_provenance.
- NP418957.RAa68LS0yuBcoUNQ1N-gCp6WSFJgT3ujxgAnXR9cOHhc4130_assertion wasDerivedFrom befree-2016 NP418957.RAa68LS0yuBcoUNQ1N-gCp6WSFJgT3ujxgAnXR9cOHhc4130_provenance.
- NP418957.RAa68LS0yuBcoUNQ1N-gCp6WSFJgT3ujxgAnXR9cOHhc4130_assertion wasGeneratedBy ECO_0000203 NP418957.RAa68LS0yuBcoUNQ1N-gCp6WSFJgT3ujxgAnXR9cOHhc4130_provenance.