@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP201000.RAsE-oyCao-xaCQmV8j8-r0dmBilFkbM8NTwG5uCwpF3w
> .
@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:NP201000.RAsE-oyCao-xaCQmV8j8-r0dmBilFkbM8NTwG5uCwpF3w130_head
{
this:
np:hasAssertion
dgn-np:NP201000.RAsE-oyCao-xaCQmV8j8-r0dmBilFkbM8NTwG5uCwpF3w130_assertion
;
np:hasProvenance
dgn-np:NP201000.RAsE-oyCao-xaCQmV8j8-r0dmBilFkbM8NTwG5uCwpF3w130_provenance
;
np:hasPublicationInfo
dgn-np:NP201000.RAsE-oyCao-xaCQmV8j8-r0dmBilFkbM8NTwG5uCwpF3w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP201000.RAsE-oyCao-xaCQmV8j8-r0dmBilFkbM8NTwG5uCwpF3w130_assertion
a
np:Assertion
.
dgn-np:NP201000.RAsE-oyCao-xaCQmV8j8-r0dmBilFkbM8NTwG5uCwpF3w130_provenance
a
np:Provenance
.
dgn-np:NP201000.RAsE-oyCao-xaCQmV8j8-r0dmBilFkbM8NTwG5uCwpF3w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP201000.RAsE-oyCao-xaCQmV8j8-r0dmBilFkbM8NTwG5uCwpF3w130_assertion
{
miriam-gene:3569
a
ncit:C16612
.
lld:C0866588
a
ncit:C7057
.
dgn-gda:DGNad2f32495ea824c4ccbd68afe7e6b7a9
sio:SIO_000628
miriam-gene:3569
,
lld:C0866588
;
a
sio:SIO_001121
.
}
dgn-np:NP201000.RAsE-oyCao-xaCQmV8j8-r0dmBilFkbM8NTwG5uCwpF3w130_provenance
{
dgn-np:NP201000.RAsE-oyCao-xaCQmV8j8-r0dmBilFkbM8NTwG5uCwpF3w130_assertion
dcterms:description
"[In the present study, we investigated the possible association of (1) a naturally occurring variable number tandem repeat (vntr) polymorphism (C allele) in the 3' flanking region of the interleukin-6 gene (IL-6), previously demonstrated to modify the course of Alzheimer's disease, systemic lupus erythematodes and Multiple Sclerosis (MS), (2) a tetranucleotide repeat polymorphism (TAAA)(n) in the 3' flanking region of the MOG gene and (3) HLA class II alleles with adult clinical phenotypes and serum antibody responses to MOG in 70 adult X-ALD patients.]. 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:12576235
;
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:NP201000.RAsE-oyCao-xaCQmV8j8-r0dmBilFkbM8NTwG5uCwpF3w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:51+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" .
}