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http://rdf.disgenet.org/nanopublications.trig#NP925378.RA7K2bS7f54rRZW_Zr806rcboD0LbXV2X5yD_hRhz1aO0
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
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np:hasAssertion
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;
np:hasProvenance
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np:Nanopublication
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a
np:Assertion
.
dgn-np:NP925378.RA7K2bS7f54rRZW_Zr806rcboD0LbXV2X5yD_hRhz1aO0130_provenance
a
np:Provenance
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dgn-np:NP925378.RA7K2bS7f54rRZW_Zr806rcboD0LbXV2X5yD_hRhz1aO0130_publicationInfo
a
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{
miriam-gene:57038
a
ncit:C16612
.
lld:C1261175
a
ncit:C7057
.
dgn-gda:DGNd74681c8744ea1867a7cdb42de202c53
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dgn-np:NP925378.RA7K2bS7f54rRZW_Zr806rcboD0LbXV2X5yD_hRhz1aO0130_provenance
{
dgn-np:NP925378.RA7K2bS7f54rRZW_Zr806rcboD0LbXV2X5yD_hRhz1aO0130_assertion
dcterms:description
"[In this review we describe the neuroradiological, neuropathological, clinical and genetic features of the different PCH subtypes and we report on in vitro and in vivo studies on the tRNA splicing endonuclease and mitochondrial arginyl-tRNA synthetase and discuss their relation to pontocerebellar hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:21749694
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP925378.RA7K2bS7f54rRZW_Zr806rcboD0LbXV2X5yD_hRhz1aO0130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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