Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_provenance.
- NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_assertion wasGeneratedBy ECO_0000203 NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_provenance.
- NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_assertion wasDerivedFrom befree-20140225 NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_provenance.
- NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_assertion SIO_000772 14594802 NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_provenance.
- NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_assertion evidence source_evidence_literature NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_provenance.
- NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_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." NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP706035.RAX9Gfx1tFyOJDvyNLXiwMWguo1XAIvAHLELx9DJK0-Pw130_provenance.