Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_provenance.
- NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_assertion description "[Recurrent somatic ASXL1 mutations occur in patients with myelodysplastic syndrome, myeloproliferative neoplasms, and acute myeloid leukemia, and are associated with adverse outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_provenance.
- NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_assertion evidence source_evidence_literature NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_provenance.
- NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_assertion SIO_000772 22897849 NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_provenance.
- NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_assertion wasDerivedFrom befree-2016 NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_provenance.
- NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_assertion wasGeneratedBy ECO_0000203 NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1005628.RA46JcQka8ay7eF7pjDjVuWiDiJSVxKnUP86kc1M5zU9o130_provenance.