@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE
> .
@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:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_head
{
this:
np:hasAssertion
dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_assertion
;
np:hasProvenance
dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_provenance
;
np:hasPublicationInfo
dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_assertion
a
np:Assertion
.
dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_provenance
a
np:Provenance
.
dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_assertion
{
miriam-gene:3565
a
ncit:C16612
.
lld:C2732618
a
ncit:C7057
.
dgn-gda:DGNb57156d89e6ba4d80a9e59c66408d1d7
sio:SIO_000628
miriam-gene:3565
,
lld:C2732618
;
a
sio:SIO_001121
.
}
dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_provenance
{
dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_assertion
dcterms:description
"[Altogether ten Single Nucleotide Polymorphisms (SNPs) of IL17A (rs2275913), IL17F (rs763780), IL4 (rs2243250), IL12A (rs583911), IL12B (rs3212227 and (rs17860508), IL23R (rs7517847), CXCL1 (rs4074), CXCL5 (rs425535) and CXCR2 (rs2230054) genes were genotyped by PCR with sequence specific primers (SSP) in 98 patients with PJI and two control groups 1) an aseptic TJA control (253 patients with TJA that did not develop PJI at least 6 yrs.]. 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:22660232
;
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:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:47+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" .
}