@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP640977.RAiBVNz-joZieeUF8OFU5Nlamn0kGmZCfqWpLxfvE6i6I
> .
@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:NP640977.RAiBVNz-joZieeUF8OFU5Nlamn0kGmZCfqWpLxfvE6i6I130_head
{
this:
np:hasAssertion
dgn-np:NP640977.RAiBVNz-joZieeUF8OFU5Nlamn0kGmZCfqWpLxfvE6i6I130_assertion
;
np:hasProvenance
dgn-np:NP640977.RAiBVNz-joZieeUF8OFU5Nlamn0kGmZCfqWpLxfvE6i6I130_provenance
;
np:hasPublicationInfo
dgn-np:NP640977.RAiBVNz-joZieeUF8OFU5Nlamn0kGmZCfqWpLxfvE6i6I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP640977.RAiBVNz-joZieeUF8OFU5Nlamn0kGmZCfqWpLxfvE6i6I130_assertion
a
np:Assertion
.
dgn-np:NP640977.RAiBVNz-joZieeUF8OFU5Nlamn0kGmZCfqWpLxfvE6i6I130_provenance
a
np:Provenance
.
dgn-np:NP640977.RAiBVNz-joZieeUF8OFU5Nlamn0kGmZCfqWpLxfvE6i6I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP640977.RAiBVNz-joZieeUF8OFU5Nlamn0kGmZCfqWpLxfvE6i6I130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGN16c1c970367304f3e5db5fe79c2dcaeb
sio:SIO_000628
miriam-gene:5621
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP640977.RAiBVNz-joZieeUF8OFU5Nlamn0kGmZCfqWpLxfvE6i6I130_provenance
{
dgn-np:NP640977.RAiBVNz-joZieeUF8OFU5Nlamn0kGmZCfqWpLxfvE6i6I130_assertion
dcterms:description
"[We hereby report a large Chinese family with P102L mutation of PRNP whose clinical manifestations at onset were intriguingly heterogeneous, either rapidly progressive dementia with scanty other neurological features or slowly progressive ataxia followed by cognitive impairment.]. 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:19696976
;
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:NP640977.RAiBVNz-joZieeUF8OFU5Nlamn0kGmZCfqWpLxfvE6i6I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
}