@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk
> .
@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:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_head
{
this:
np:hasAssertion
dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_assertion
;
np:hasProvenance
dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_provenance
;
np:hasPublicationInfo
dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_assertion
a
np:Assertion
.
dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_provenance
a
np:Provenance
.
dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_assertion
{
miriam-gene:8170
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN517236630313a2925ca8f0a8c48b5075
sio:SIO_000628
miriam-gene:8170
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_provenance
{
dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_assertion
dcterms:description
"[To determine whether non-missense genetic polymorphisms located in regulatory region of TLR4 are related to RA in a Chinese Han population, four single nucleotide polymorphisms (SNPs) situated on 3' untranslating region (UTR) and 5' UTR were genotyped in 213 RA patients and 247 unrelated ethnically matched controls using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and direct sequencing techniques.]. 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:23129427
;
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:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:46+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" .
}