@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_assertion
a
np:Assertion
.
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a
np:Provenance
.
dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:3123
a
ncit:C16612
.
lld:C0007099
a
ncit:C7057
.
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sio:SIO_000628
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,
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.
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dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_provenance
{
dgn-np:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_assertion
dcterms:description
"[We genotyped the human leukocyte antigens HLA-DRB1 and HLA-A, plus a panel of single nucleotide polymorphisms (SNPs) that have been associated with susceptibility to MS and then correlated the genotypes with the levels of CXCL13, as measured with ELISA in the CSF of a total of 663 patients with MS, CIS, other neurological diseases (OND) or OND with an inflammatory component (iOND).]. 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:23175382
;
prov:wasDerivedFrom
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;
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:NP674146.RAFVCjHkeEiNK3tlWL8qbf4KOsw8Sw2dtst-dIEqjhHpE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:47+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
dgn-void:disgenetrdf
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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pav:version
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