@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP854692.RAl7Fy_jOIZboO-5uEKmwuHbppr6ZE6setXVGIfxcRIKg
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP854692.RAl7Fy_jOIZboO-5uEKmwuHbppr6ZE6setXVGIfxcRIKg130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP854692.RAl7Fy_jOIZboO-5uEKmwuHbppr6ZE6setXVGIfxcRIKg130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP854692.RAl7Fy_jOIZboO-5uEKmwuHbppr6ZE6setXVGIfxcRIKg130_assertion
a
np:Assertion
.
dgn-np:NP854692.RAl7Fy_jOIZboO-5uEKmwuHbppr6ZE6setXVGIfxcRIKg130_provenance
a
np:Provenance
.
dgn-np:NP854692.RAl7Fy_jOIZboO-5uEKmwuHbppr6ZE6setXVGIfxcRIKg130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP854692.RAl7Fy_jOIZboO-5uEKmwuHbppr6ZE6setXVGIfxcRIKg130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0011265
a
ncit:C7057
.
dgn-gda:DGNe2504d33791faea26adf93dd13657f97
sio:SIO_000628
miriam-gene:5621
,
lld:C0011265
;
a
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.
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dgn-np:NP854692.RAl7Fy_jOIZboO-5uEKmwuHbppr6ZE6setXVGIfxcRIKg130_provenance
{
dgn-np:NP854692.RAl7Fy_jOIZboO-5uEKmwuHbppr6ZE6setXVGIfxcRIKg130_assertion
dcterms:description
"[This case supports the pathogenicity of the T188 PRNP mutation, demonstrates the variability of clinical phenotypes associated with certain mutations, and emphasizes the importance of testing for genetic prion disease in cases of apparently sporadic atypical dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:21107135
;
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:NP854692.RAl7Fy_jOIZboO-5uEKmwuHbppr6ZE6setXVGIfxcRIKg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:12+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
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" .
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"v4.0.0" .
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