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> .
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> .
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http://identifiers.org/ncbigene/
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http://identifiers.org/pubmed/
> .
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> .
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http://purl.org/ontology/wi/core#
> .
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http://www.w3.org/ns/prov#
> .
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http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
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http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
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http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
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.
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miriam-gene:6201
a
ncit:C16612
.
lld:C0398550
a
ncit:C7057
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dgn-np:NP499431.RABnoBTBIoEBdLIL2dRGge_f5UqptO-NP2lrrqscjqccA130_assertion
dcterms:description
"[We also demonstrate that mutations of RPL5, RPL11, or RPS7 in DBA cells is associated with diverse defects in the maturation of ribosomal RNAs in the large or the small ribosomal subunit production pathway, expanding the repertoire of ribosomal RNA processing defects associated with DBA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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xsd:date
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dgn-void:source_evidence_literature
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{
this:
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xsd:dateTime
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