Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_provenance.
- NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_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." NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_provenance.
- NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_assertion evidence source_evidence_literature NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_provenance.
- NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_assertion SIO_000772 22897849 NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_provenance.
- NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_assertion wasDerivedFrom befree-20140225 NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_provenance.
- NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_assertion wasGeneratedBy ECO_0000203 NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP815407.RAkFVBfKhFPRdSTh5FXdTNqFcBC0saCc-k0RbxmhRV38k130_provenance.