Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_provenance.
- NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_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." NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_provenance.
- NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_assertion evidence source_evidence_literature NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_provenance.
- NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_assertion SIO_000772 22897849 NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_provenance.
- NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_assertion wasDerivedFrom befree-20150227 NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_provenance.
- NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_assertion wasGeneratedBy ECO_0000203 NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978726.RAi0UD2X-4kE_bnPwjGbmWKisqBMc5tqFyGnlZevYqowU130_provenance.