Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP622995.RA5kP9SZn3BVnCyVPvqDA2GolbEszmzoF7mgdYvtKjC0o130_provenance.