Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_provenance.
- NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_assertion description "[Recently, the 5q- syndrome, a subtype of myelodysplastic syndrome characterized by a defect in erythroid differentiation, is caused by a somatically acquired deletion of chromosome 5q, which results in haploinsufficiency of RPS14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_provenance.
- NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_assertion evidence source_evidence_literature NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_provenance.
- NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_assertion SIO_000772 20882441 NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_provenance.
- NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_assertion wasDerivedFrom befree-20140225 NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_provenance.
- NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_assertion wasGeneratedBy ECO_0000203 NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP583186.RAmtG9M92YV579GKy9JcAP3JXIWxl2EnlU2KX-bPAOWMA130_provenance.