@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1089769.RAdetYbU3gFcOoCuVZXBzTfFWKanwOUGV-vNUtP1eXm8A
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1089769.RAdetYbU3gFcOoCuVZXBzTfFWKanwOUGV-vNUtP1eXm8A130_head
{
this:
np:hasAssertion
dgn-np:NP1089769.RAdetYbU3gFcOoCuVZXBzTfFWKanwOUGV-vNUtP1eXm8A130_assertion
;
np:hasProvenance
dgn-np:NP1089769.RAdetYbU3gFcOoCuVZXBzTfFWKanwOUGV-vNUtP1eXm8A130_provenance
;
np:hasPublicationInfo
dgn-np:NP1089769.RAdetYbU3gFcOoCuVZXBzTfFWKanwOUGV-vNUtP1eXm8A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1089769.RAdetYbU3gFcOoCuVZXBzTfFWKanwOUGV-vNUtP1eXm8A130_assertion
a
np:Assertion
.
dgn-np:NP1089769.RAdetYbU3gFcOoCuVZXBzTfFWKanwOUGV-vNUtP1eXm8A130_provenance
a
np:Provenance
.
dgn-np:NP1089769.RAdetYbU3gFcOoCuVZXBzTfFWKanwOUGV-vNUtP1eXm8A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1089769.RAdetYbU3gFcOoCuVZXBzTfFWKanwOUGV-vNUtP1eXm8A130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGNe6279d47f0e425f043f384f9aaa7b5c2
sio:SIO_000628
miriam-gene:5621
,
lld:C0524851
;
a
sio:SIO_001121
.
}
dgn-np:NP1089769.RAdetYbU3gFcOoCuVZXBzTfFWKanwOUGV-vNUtP1eXm8A130_provenance
{
dgn-np:NP1089769.RAdetYbU3gFcOoCuVZXBzTfFWKanwOUGV-vNUtP1eXm8A130_assertion
dcterms:description
"[Genetic Creutzfeldt-Jakob disease, Gerstmann-Sträussler-Scheinker syndrome, fatal familial insomnia and prion protein cerebral amyloid angiopathy are clinically and neuropathologically distinct neurodegenerative diseases linked to mutations in the PRNP gene encoding the cellular prion protein (PrPC).]. 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:23808898
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1089769.RAdetYbU3gFcOoCuVZXBzTfFWKanwOUGV-vNUtP1eXm8A130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:00+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}