@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP128367.RAbanHiXohKpx8jmVTzmI2PlNlJ9hyMb91nVvL9ha_oIA
> .
@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:NP128367.RAbanHiXohKpx8jmVTzmI2PlNlJ9hyMb91nVvL9ha_oIA130_head
{
this:
np:hasAssertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP128367.RAbanHiXohKpx8jmVTzmI2PlNlJ9hyMb91nVvL9ha_oIA130_publicationInfo
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a
np:Nanopublication
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a
np:Assertion
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np:Provenance
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{
miriam-gene:26191
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGNd9e3c5257519fd133c0f18e968b0437d
sio:SIO_000628
miriam-gene:26191
,
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;
a
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.
}
dgn-np:NP128367.RAbanHiXohKpx8jmVTzmI2PlNlJ9hyMb91nVvL9ha_oIA130_provenance
{
dgn-np:NP128367.RAbanHiXohKpx8jmVTzmI2PlNlJ9hyMb91nVvL9ha_oIA130_assertion
dcterms:description
"[Cox proportional hazards regression models were used to assess the association of the HLA-DRB1 (including the shared epitope SE) and PTPN22 genes with the risk of death from all causes and from cardiovascular disease (CVD) and to assess the interactions between SE, smoking, and anti-cyclic citrullinated peptide (anti-CCP) status, adjusted by age at symptom onset and sex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:18240242
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prov:wasDerivedFrom
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prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP128367.RAbanHiXohKpx8jmVTzmI2PlNlJ9hyMb91nVvL9ha_oIA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:52+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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pav:authoredBy
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> , <
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> , <
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> , <
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<
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pav:version
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