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- source_evidence_literature type ECO_0000212 NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_provenance.
- NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_assertion description "[Complex karyotypes are seen in approximately 15% of de novo MDS/AML and in up to 50% of therapy-related MDS/AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_provenance.
- NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_assertion evidence source_evidence_literature NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_provenance.
- NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_assertion SIO_000772 16142824 NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_provenance.
- NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_assertion wasDerivedFrom befree-20150227 NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_provenance.
- NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_assertion wasGeneratedBy ECO_0000203 NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978678.RAuy1Cf_f8w9ojLgi-dFEfh0LOgL9hZBMjc2ATgBwMtHI130_provenance.