@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k
> .
@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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{
this:
np:hasAssertion
dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion
;
np:hasProvenance
dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance
;
np:hasPublicationInfo
dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion
a
np:Assertion
.
dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance
a
np:Provenance
.
dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion
{
miriam-gene:23627
a
ncit:C16612
.
lld:C2931859
a
ncit:C7057
.
dgn-gda:DGN0b8df29bada3516237aeb88a911a742f
sio:SIO_000628
miriam-gene:23627
,
lld:C2931859
;
a
sio:SIO_001121
.
}
dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance
{
dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion
dcterms:description
"[To investigate whether the PRND polymorphisms are associated with an increased risk for developing sporadic CJD in the Korean population, we compared the genotype and allele frequencies of PRND polymorphisms in 110 sporadic CJD patients with those in 102 healthy Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:15933804
;
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:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:09+02:00"^^
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
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
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"v2.1.0" .
}