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- source_evidence_literature type ECO_0000212 NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_provenance.
- NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_assertion description "[We found a high incidence of ASXL1 mutation in MF patients (20%) and a low incidence in PV (7%) and ET (4%) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_provenance.
- NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_assertion evidence source_evidence_literature NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_provenance.
- NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_assertion SIO_000772 22489043 NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_provenance.
- NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_assertion wasDerivedFrom befree-20150227 NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_provenance.
- NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_assertion wasGeneratedBy ECO_0000203 NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978579.RAYWC9AUJbF4KUWMsBW-fDs2C_A0ypUKIydNyBBmMaQu0130_provenance.