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- source_evidence_literature type ECO_0000212 NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_provenance.
- NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_assertion description "[In conclusion, within MDS/MPN, the World Health Organization 2008 criteria for aCML identify a subgroup of patients with features clearly distinct from MDS/MPN-U.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_provenance.
- NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_assertion evidence source_evidence_literature NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_provenance.
- NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_assertion SIO_000772 24627528 NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_provenance.
- NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_assertion wasDerivedFrom befree-20150227 NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_provenance.
- NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_assertion wasGeneratedBy ECO_0000203 NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914196.RAHa0q3bgb7fF83kQR9tgpc1-_uf--TuQTwzqqM13VacY130_provenance.