Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_provenance.
- befree-2016 importedOn "2016-02-19" NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_provenance.
- NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_assertion wasGeneratedBy ECO_0000203 NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_provenance.
- NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_assertion wasDerivedFrom befree-2016 NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_provenance.
- NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_assertion SIO_000772 14594802 NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_provenance.
- NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_assertion evidence source_evidence_literature NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_provenance.
- NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_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." NP418958.RAfyVwVfTtosh_-ylalK4qNXxwQCtUNM_9tKAGIW4lUX4130_provenance.