@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP206968.RAGSfxLQk663JdPz2labIIjHTqBwo5kgE4nX47LMtZISU
> .
@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:NP206968.RAGSfxLQk663JdPz2labIIjHTqBwo5kgE4nX47LMtZISU130_head
{
this:
np:hasAssertion
dgn-np:NP206968.RAGSfxLQk663JdPz2labIIjHTqBwo5kgE4nX47LMtZISU130_assertion
;
np:hasProvenance
dgn-np:NP206968.RAGSfxLQk663JdPz2labIIjHTqBwo5kgE4nX47LMtZISU130_provenance
;
np:hasPublicationInfo
dgn-np:NP206968.RAGSfxLQk663JdPz2labIIjHTqBwo5kgE4nX47LMtZISU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP206968.RAGSfxLQk663JdPz2labIIjHTqBwo5kgE4nX47LMtZISU130_assertion
a
np:Assertion
.
dgn-np:NP206968.RAGSfxLQk663JdPz2labIIjHTqBwo5kgE4nX47LMtZISU130_provenance
a
np:Provenance
.
dgn-np:NP206968.RAGSfxLQk663JdPz2labIIjHTqBwo5kgE4nX47LMtZISU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP206968.RAGSfxLQk663JdPz2labIIjHTqBwo5kgE4nX47LMtZISU130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0042373
a
ncit:C7057
.
dgn-gda:DGN678acd7cce565297e67d27a8f389c089
sio:SIO_000628
miriam-gene:348
,
lld:C0042373
;
a
sio:SIO_001121
.
}
dgn-np:NP206968.RAGSfxLQk663JdPz2labIIjHTqBwo5kgE4nX47LMtZISU130_provenance
{
dgn-np:NP206968.RAGSfxLQk663JdPz2labIIjHTqBwo5kgE4nX47LMtZISU130_assertion
dcterms:description
"[In summary, the epsilon2 allele was in linkage disequilibrium with the -427C allele in all studied groups, and only slight associations between the analyzed APOE polymorphisms in the promoter and in the coding region and carotid and coronary vascular disease have been observed.]. 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:18219091
;
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:NP206968.RAGSfxLQk663JdPz2labIIjHTqBwo5kgE4nX47LMtZISU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:54+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" .
}