@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ
> .
@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#
> .
dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_head
{
this:
np:hasAssertion
dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_assertion
;
np:hasProvenance
dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_assertion
a
np:Assertion
.
dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_provenance
a
np:Provenance
.
dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0162534
a
ncit:C7057
.
dgn-gda:DGN40951720da1a461b1b3279e07cf4aa53
sio:SIO_000628
miriam-gene:5621
,
lld:C0162534
;
a
sio:SIO_001122
.
}
dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_provenance
{
dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_assertion
dcterms:description
"[ The results of this study confirm that the different polymorphism at codon 129 of the PRNP gene, which could be involved in the structural domains of human PrP, might modulate the pathological phenotype of TSE.]. 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:11220690
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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
pav:version
"v2.1.0" .
}