Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_provenance.
- NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_assertion description "[A systematic RNA interference screen to interrogate the function of each gene in the common deleted region (CDR) for the 5q- syndrome identified RPS14 as a critical haploinsufficiency disease gene for the erythroid failure, which is a characteristic of this syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_provenance.
- NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_assertion evidence source_evidence_literature NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_provenance.
- NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_assertion SIO_000772 19322210 NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_provenance.
- NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_assertion wasDerivedFrom befree-20140225 NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_provenance.
- NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_assertion wasGeneratedBy ECO_0000203 NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP840518.RAJk8WDL5e8rDLe6ajG8mzUnkRtdoahJuGrmkDLGPQUa4130_provenance.