Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_provenance.
- NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_assertion description "[In up to 70% of patients with MDS clonal chromosome abnormalities can be identified which have a high impact on setting the correct diagnosis and estimation of prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_provenance.
- NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_assertion evidence source_evidence_literature NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_provenance.
- NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_assertion SIO_000772 24507811 NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_provenance.
- NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_assertion wasDerivedFrom befree-20150227 NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_provenance.
- NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_assertion wasGeneratedBy ECO_0000203 NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP913928.RATEmYk_4tHMSM41VaVT_hGlfr4C0_lBtC_SQuIlnecjE130_provenance.