Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_assertion> ?p ?o ?g. }
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- NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_assertion type Assertion NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_head.
- NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_assertion description "[We identified nonsense mutations or hemizygous deletion of ASXL1 in 36% of the patients with myelofibrosis, but very rarely among those with polycythemia vera or essential thrombocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_provenance.
- NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_assertion evidence source_evidence_literature NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_provenance.
- NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_assertion SIO_000772 21712540 NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_provenance.
- NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_assertion wasDerivedFrom befree-20140225 NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_provenance.
- NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_assertion wasGeneratedBy ECO_0000203 NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_provenance.