@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP688598.RAbSxpBvWWLl8AElmeNmiOzxqO_b_7DojgY7QVXU_TA9Y
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP688598.RAbSxpBvWWLl8AElmeNmiOzxqO_b_7DojgY7QVXU_TA9Y130_head
{
this:
np:hasAssertion
dgn-np:NP688598.RAbSxpBvWWLl8AElmeNmiOzxqO_b_7DojgY7QVXU_TA9Y130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP688598.RAbSxpBvWWLl8AElmeNmiOzxqO_b_7DojgY7QVXU_TA9Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP688598.RAbSxpBvWWLl8AElmeNmiOzxqO_b_7DojgY7QVXU_TA9Y130_assertion
a
np:Assertion
.
dgn-np:NP688598.RAbSxpBvWWLl8AElmeNmiOzxqO_b_7DojgY7QVXU_TA9Y130_provenance
a
np:Provenance
.
dgn-np:NP688598.RAbSxpBvWWLl8AElmeNmiOzxqO_b_7DojgY7QVXU_TA9Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP688598.RAbSxpBvWWLl8AElmeNmiOzxqO_b_7DojgY7QVXU_TA9Y130_assertion
{
miriam-gene:6387
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNbb917466786463e385590e0f1fe9d633
sio:SIO_000628
miriam-gene:6387
,
lld:C1956346
;
a
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.
}
dgn-np:NP688598.RAbSxpBvWWLl8AElmeNmiOzxqO_b_7DojgY7QVXU_TA9Y130_provenance
{
dgn-np:NP688598.RAbSxpBvWWLl8AElmeNmiOzxqO_b_7DojgY7QVXU_TA9Y130_assertion
dcterms:description
"[Because previous genome-wide association studies demonstrated an association between CXCL12 rs501120 and coronary artery disease, in the present study we assessed the potential association of this polymorphism with the risk of cardiovascular (CV) disease in 1,321 Spanish patients with RA.]. 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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP688598.RAbSxpBvWWLl8AElmeNmiOzxqO_b_7DojgY7QVXU_TA9Y130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:35+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
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;
pav:authoredBy
<
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> , <
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> , <
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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
}