Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_provenance.
- NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_assertion description "[In particular, ASXL1 mutations are common in patients with hematologic malignancies associated with myelodysplasia, including myelodysplastic syndromes (MDSs), and chronic myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_provenance.
- NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_assertion evidence source_evidence_literature NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_provenance.
- NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_assertion SIO_000772 24216483 NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_provenance.
- NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_assertion wasDerivedFrom befree-20150227 NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_provenance.
- NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_assertion wasGeneratedBy ECO_0000203 NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978632.RA2S3-CrFxB_G5FoCU-TAg8e5Db7q5_7WRRmFOhWIT2Ko130_provenance.