Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_provenance.
- NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_assertion description "[It is now recognized that p53 activation, caused by haploinsufficiency for the ribosomal gene RPS14 (mapping to the commonly deleted region), is the probable cause of the erythroid defect in the 5q- syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_provenance.
- NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_assertion evidence source_evidence_literature NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_provenance.
- NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_assertion SIO_000772 22571696 NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_provenance.
- NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_assertion wasDerivedFrom befree-2016 NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_provenance.
- NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_assertion wasGeneratedBy ECO_0000203 NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_provenance.
- befree-2016 importedOn "2016-02-19" NP980764.RA6SvoCyCKOKqJY2MuUqRztNQ4YDdrmgn0CSdfd-GCcsE130_provenance.