@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP418943.RAyIjZqzDOrOSVZGhSYR9ld2LU9bM3L7c6cCzomglmQFE
> .
@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:NP418943.RAyIjZqzDOrOSVZGhSYR9ld2LU9bM3L7c6cCzomglmQFE130_head
{
this:
np:hasAssertion
dgn-np:NP418943.RAyIjZqzDOrOSVZGhSYR9ld2LU9bM3L7c6cCzomglmQFE130_assertion
;
np:hasProvenance
dgn-np:NP418943.RAyIjZqzDOrOSVZGhSYR9ld2LU9bM3L7c6cCzomglmQFE130_provenance
;
np:hasPublicationInfo
dgn-np:NP418943.RAyIjZqzDOrOSVZGhSYR9ld2LU9bM3L7c6cCzomglmQFE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP418943.RAyIjZqzDOrOSVZGhSYR9ld2LU9bM3L7c6cCzomglmQFE130_assertion
a
np:Assertion
.
dgn-np:NP418943.RAyIjZqzDOrOSVZGhSYR9ld2LU9bM3L7c6cCzomglmQFE130_provenance
a
np:Provenance
.
dgn-np:NP418943.RAyIjZqzDOrOSVZGhSYR9ld2LU9bM3L7c6cCzomglmQFE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP418943.RAyIjZqzDOrOSVZGhSYR9ld2LU9bM3L7c6cCzomglmQFE130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0233763
a
ncit:C7057
.
dgn-gda:DGN2f79494f704c7bc7e83a98b226a92458
sio:SIO_000628
miriam-gene:348
,
lld:C0233763
;
a
sio:SIO_001121
.
}
dgn-np:NP418943.RAyIjZqzDOrOSVZGhSYR9ld2LU9bM3L7c6cCzomglmQFE130_provenance
{
dgn-np:NP418943.RAyIjZqzDOrOSVZGhSYR9ld2LU9bM3L7c6cCzomglmQFE130_assertion
dcterms:description
"[To determine whether the frequency of dopamine receptor genetic variants and APOE alleles in patients with PD with and without chronic visual hallucinations resembles the pattern previously documented in patients with Alzheimer disease.]. 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:11176958
;
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:NP418943.RAyIjZqzDOrOSVZGhSYR9ld2LU9bM3L7c6cCzomglmQFE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:08+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" .
}