@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U
> .
@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:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_head
{
this:
np:hasAssertion
dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_assertion
;
np:hasProvenance
dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_provenance
;
np:hasPublicationInfo
dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_assertion
a
np:Assertion
.
dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_provenance
a
np:Provenance
.
dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_assertion
{
miriam-gene:6387
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGNc3d3b1bea059fdf55da7fdfbad849686
sio:SIO_000628
miriam-gene:6387
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_provenance
{
dgn-np:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_assertion
dcterms:description
"[However, no significant differences in genotypic and allelic frequencies between RA patients with and without CV events were observed, as was also the case when values of surrogate markers of atherosclerosis were assessed according to CXCL12 rs501120 genotype frequencies.]. 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:22386691
;
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:NP939742.RAral5kNCBMKe6hNePQW0E8i_SHS8-KCeHHeNSzSPu48U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}