@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP111026.RAqLasLQdI1uF0BsRi8C-35OxjseINC9Bjlwp7dfQHyBY
> .
@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:NP111026.RAqLasLQdI1uF0BsRi8C-35OxjseINC9Bjlwp7dfQHyBY130_head
{
this:
np:hasAssertion
dgn-np:NP111026.RAqLasLQdI1uF0BsRi8C-35OxjseINC9Bjlwp7dfQHyBY130_assertion
;
np:hasProvenance
dgn-np:NP111026.RAqLasLQdI1uF0BsRi8C-35OxjseINC9Bjlwp7dfQHyBY130_provenance
;
np:hasPublicationInfo
dgn-np:NP111026.RAqLasLQdI1uF0BsRi8C-35OxjseINC9Bjlwp7dfQHyBY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP111026.RAqLasLQdI1uF0BsRi8C-35OxjseINC9Bjlwp7dfQHyBY130_assertion
a
np:Assertion
.
dgn-np:NP111026.RAqLasLQdI1uF0BsRi8C-35OxjseINC9Bjlwp7dfQHyBY130_provenance
a
np:Provenance
.
dgn-np:NP111026.RAqLasLQdI1uF0BsRi8C-35OxjseINC9Bjlwp7dfQHyBY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP111026.RAqLasLQdI1uF0BsRi8C-35OxjseINC9Bjlwp7dfQHyBY130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0242422
a
ncit:C7057
.
dgn-gda:DGNd82a6d4f6114c31e97cf8b751c6547af
sio:SIO_000628
miriam-gene:4137
,
lld:C0242422
;
a
sio:SIO_001122
.
}
dgn-np:NP111026.RAqLasLQdI1uF0BsRi8C-35OxjseINC9Bjlwp7dfQHyBY130_provenance
{
dgn-np:NP111026.RAqLasLQdI1uF0BsRi8C-35OxjseINC9Bjlwp7dfQHyBY130_assertion
dcterms:description
"[The phenotype of pallidopontonigral degeneration (PPND) resulting from N279K mutation of tau includes dysfunction of the autonomic nervous system, correlating with the duration of illness and clinical and functional severity of parkinsonism.]. 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:12492138
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP111026.RAqLasLQdI1uF0BsRi8C-35OxjseINC9Bjlwp7dfQHyBY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:56+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" .
}