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- source_evidence_literature type ECO_0000212 NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_provenance.
- NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_assertion description "[In univariate analysis, the presence of C-findings, the AHNMD subtypes (SM-MDS/CMML/AML versus SM-MPN/hypereosinophilia) (p?=?0.044), Neutropenia (p?=?0.015), high monocyte level (p?=?0.015) and the presence of ASXL1 mutation had detrimental effects on OS (p?=?0.007).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_provenance.
- NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_assertion evidence source_evidence_literature NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_provenance.
- NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_assertion SIO_000772 24465546 NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_provenance.
- NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_assertion wasDerivedFrom befree-20150227 NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_provenance.
- NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_assertion wasGeneratedBy ECO_0000203 NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978556.RA08Cn_igSeyvbj0CT0jGv3I7d6qBLNARaoUeWORaGhdM130_provenance.