@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo
> .
@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:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_head
{
this:
np:hasAssertion
dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_assertion
;
np:hasProvenance
dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_provenance
;
np:hasPublicationInfo
dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_assertion
a
np:Assertion
.
dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_provenance
a
np:Provenance
.
dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_assertion
{
miriam-gene:10544
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN1a004e2120ff35ca78076439dc4b04a1
sio:SIO_000628
miriam-gene:10544
,
lld:C0038454
;
a
sio:SIO_001122
.
}
dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_provenance
{
dgn-np:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_assertion
dcterms:description
"[None of the patients with sEPCR levels below 100 ng/ml carried the A3 haplotype, while patients with elevated sEPCR levels carried the A3 haplotype either in a heterozygous or homozygous state. Our study confirms that there is a strong association between A3 haplotype and elevated sEPCR levels. We suggest that elevated sEPCR levels might increase the risk of stroke at pediatric age when compared to controls. Studies with large series of patients are warranted to confirm this hypothesis.]. 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:17027065
;
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:NP66325.RAgyJhp2ksScnGxpz3plBkB8epFXHgP4zSYztBZjCMsAo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:31+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" .
}