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- source_evidence_literature type ECO_0000212 NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_provenance.
- NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_assertion description "[Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_provenance.
- NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_assertion evidence source_evidence_literature NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_provenance.
- NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_assertion SIO_000772 24218140 NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_provenance.
- NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_assertion wasDerivedFrom befree-20150227 NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_provenance.
- NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_assertion wasGeneratedBy ECO_0000203 NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978537.RA9TJoHgbuKW0qTfKwghEiSJEYCHGeAvSIvfmGRDWEgYg130_provenance.