@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP342191.RAVK4HLsERwZ8von50Y4wjQS9q1jryl799lrGcAbyFy9U
> .
@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:NP342191.RAVK4HLsERwZ8von50Y4wjQS9q1jryl799lrGcAbyFy9U130_head
{
this:
np:hasAssertion
dgn-np:NP342191.RAVK4HLsERwZ8von50Y4wjQS9q1jryl799lrGcAbyFy9U130_assertion
;
np:hasProvenance
dgn-np:NP342191.RAVK4HLsERwZ8von50Y4wjQS9q1jryl799lrGcAbyFy9U130_provenance
;
np:hasPublicationInfo
dgn-np:NP342191.RAVK4HLsERwZ8von50Y4wjQS9q1jryl799lrGcAbyFy9U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP342191.RAVK4HLsERwZ8von50Y4wjQS9q1jryl799lrGcAbyFy9U130_assertion
a
np:Assertion
.
dgn-np:NP342191.RAVK4HLsERwZ8von50Y4wjQS9q1jryl799lrGcAbyFy9U130_provenance
a
np:Provenance
.
dgn-np:NP342191.RAVK4HLsERwZ8von50Y4wjQS9q1jryl799lrGcAbyFy9U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP342191.RAVK4HLsERwZ8von50Y4wjQS9q1jryl799lrGcAbyFy9U130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0020476
a
ncit:C7057
.
dgn-gda:DGN4eb963b4159b7f6b929e3145d3be3205
sio:SIO_000628
miriam-gene:348
,
lld:C0020476
;
a
sio:SIO_001121
.
}
dgn-np:NP342191.RAVK4HLsERwZ8von50Y4wjQS9q1jryl799lrGcAbyFy9U130_provenance
{
dgn-np:NP342191.RAVK4HLsERwZ8von50Y4wjQS9q1jryl799lrGcAbyFy9U130_assertion
dcterms:description
"[Common apoE alleles are in association with an increase in risk for central nervous and cardiovascular diseases such as Alzheimer's disease, dementia, multiple sclerosis, atherosclerosis, coronary heart disease, hyperlipoproteinemia and stroke.]. 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:17594534
;
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:NP342191.RAVK4HLsERwZ8von50Y4wjQS9q1jryl799lrGcAbyFy9U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:21+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" .
}