@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP69479.RARGRQjpoM-t1mELj0mI7co4VYy3ri2YI9zbXMEhJNCLI
> .
@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/v3.0.0/void/
> .
dgn-np:NP69479.RARGRQjpoM-t1mELj0mI7co4VYy3ri2YI9zbXMEhJNCLI130_head
{
this:
np:hasAssertion
dgn-np:NP69479.RARGRQjpoM-t1mELj0mI7co4VYy3ri2YI9zbXMEhJNCLI130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP69479.RARGRQjpoM-t1mELj0mI7co4VYy3ri2YI9zbXMEhJNCLI130_assertion
a
np:Assertion
.
dgn-np:NP69479.RARGRQjpoM-t1mELj0mI7co4VYy3ri2YI9zbXMEhJNCLI130_provenance
a
np:Provenance
.
dgn-np:NP69479.RARGRQjpoM-t1mELj0mI7co4VYy3ri2YI9zbXMEhJNCLI130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:4035
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN65217c847efa0b927c29610ba8a53f75
sio:SIO_000628
miriam-gene:4035
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP69479.RARGRQjpoM-t1mELj0mI7co4VYy3ri2YI9zbXMEhJNCLI130_provenance
{
dgn-np:NP69479.RARGRQjpoM-t1mELj0mI7co4VYy3ri2YI9zbXMEhJNCLI130_assertion
dcterms:description
"[In a case-control study in 246 AD patients and 237 healthy controls, we examined whether the combined gene effects between tau (intron 9, rs2471738) polymorphism and LRP1 (exon 3, rs1799986) polymorphism might be responsible for susceptibility to AD, independently or in concert with the APOE epsilon4 allele.]. 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:19684401
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP69479.RARGRQjpoM-t1mELj0mI7co4VYy3ri2YI9zbXMEhJNCLI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:18+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
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
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> ;
pav:createdBy
<
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> ;
pav:version
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"v3.0.0" .
}