@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_assertion
;
np:hasProvenance
dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_provenance
;
np:hasPublicationInfo
dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_assertion
a
np:Assertion
.
dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_provenance
a
np:Provenance
.
dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_assertion
{
miriam-gene:5663
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGN6705e383b49a1bfb2f4068d91a4ac2c5
sio:SIO_000628
miriam-gene:5663
,
lld:C0497327
;
a
sio:SIO_001122
.
}
dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_provenance
{
dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_assertion
dcterms:description
"[ This method provides excellent robustness, speed, and accuracy, and is well suited for determination of the polymorphism in both small and large numbers of samples. This assay could help to overcome the controversy regarding the association between the PS1 s165932 intronic polymorphism and Alzheimer's 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:16139258
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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
<
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> , <
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" .
}