@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP212988.RAYT9tVdXXNjJwHHb1LBPn3gdMf1lDnIm4DSn_0r8Mgh0
> .
@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:NP212988.RAYT9tVdXXNjJwHHb1LBPn3gdMf1lDnIm4DSn_0r8Mgh0130_head
{
this:
np:hasAssertion
dgn-np:NP212988.RAYT9tVdXXNjJwHHb1LBPn3gdMf1lDnIm4DSn_0r8Mgh0130_assertion
;
np:hasProvenance
dgn-np:NP212988.RAYT9tVdXXNjJwHHb1LBPn3gdMf1lDnIm4DSn_0r8Mgh0130_provenance
;
np:hasPublicationInfo
dgn-np:NP212988.RAYT9tVdXXNjJwHHb1LBPn3gdMf1lDnIm4DSn_0r8Mgh0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP212988.RAYT9tVdXXNjJwHHb1LBPn3gdMf1lDnIm4DSn_0r8Mgh0130_assertion
a
np:Assertion
.
dgn-np:NP212988.RAYT9tVdXXNjJwHHb1LBPn3gdMf1lDnIm4DSn_0r8Mgh0130_provenance
a
np:Provenance
.
dgn-np:NP212988.RAYT9tVdXXNjJwHHb1LBPn3gdMf1lDnIm4DSn_0r8Mgh0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP212988.RAYT9tVdXXNjJwHHb1LBPn3gdMf1lDnIm4DSn_0r8Mgh0130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGNdb790eb3fe2e261366a7e36ea0a4bff7
sio:SIO_000628
miriam-gene:348
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP212988.RAYT9tVdXXNjJwHHb1LBPn3gdMf1lDnIm4DSn_0r8Mgh0130_provenance
{
dgn-np:NP212988.RAYT9tVdXXNjJwHHb1LBPn3gdMf1lDnIm4DSn_0r8Mgh0130_assertion
dcterms:description
"[Cox proportional hazards regression models were constructed to estimate the risk for dementia in terms of relative risks (RRs) for stroke and the APOE epsilon4 allele, with adjustment for age, sex, education, systolic blood pressure, antihypertensive medication use, and heart 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:10625715
;
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:NP212988.RAYT9tVdXXNjJwHHb1LBPn3gdMf1lDnIm4DSn_0r8Mgh0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:58+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" .
}