@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78
> .
@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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_assertion
;
np:hasProvenance
dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_provenance
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np:hasPublicationInfo
dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_assertion
a
np:Assertion
.
dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_provenance
a
np:Provenance
.
dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:6387
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN83d6dfe6669fd5daa816016b7f884a31
sio:SIO_000628
miriam-gene:6387
,
lld:C0010054
;
a
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.
}
dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_provenance
{
dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_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-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:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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
<
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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
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"v2.1.0" .
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