@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP56575.RAKw69IidSCZj2eYTtA9KQgSdyxSBtxHpXF0uQfe0fZqA
> .
@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
dgn-np:NP56575.RAKw69IidSCZj2eYTtA9KQgSdyxSBtxHpXF0uQfe0fZqA130_assertion
;
np:hasProvenance
dgn-np:NP56575.RAKw69IidSCZj2eYTtA9KQgSdyxSBtxHpXF0uQfe0fZqA130_provenance
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np:hasPublicationInfo
dgn-np:NP56575.RAKw69IidSCZj2eYTtA9KQgSdyxSBtxHpXF0uQfe0fZqA130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP56575.RAKw69IidSCZj2eYTtA9KQgSdyxSBtxHpXF0uQfe0fZqA130_provenance
a
np:Provenance
.
dgn-np:NP56575.RAKw69IidSCZj2eYTtA9KQgSdyxSBtxHpXF0uQfe0fZqA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP56575.RAKw69IidSCZj2eYTtA9KQgSdyxSBtxHpXF0uQfe0fZqA130_assertion
{
miriam-gene:3606
a
ncit:C16612
.
lld:C0011615
a
ncit:C7057
.
dgn-gda:DGN2ec0a97db019b7b42395fad707d61797
sio:SIO_000628
miriam-gene:3606
,
lld:C0011615
;
a
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.
}
dgn-np:NP56575.RAKw69IidSCZj2eYTtA9KQgSdyxSBtxHpXF0uQfe0fZqA130_provenance
{
dgn-np:NP56575.RAKw69IidSCZj2eYTtA9KQgSdyxSBtxHpXF0uQfe0fZqA130_assertion
dcterms:description
"[To evaluate associations of polymorphisms in the IL18 gene on chromosome 11q22 with AE, we performed genotyping for single nucleotide polymorphisms (SNPs) in the IL18 gene in 225 patients with AE and 175 healthy control volunteers.]. 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:15806006
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP56575.RAKw69IidSCZj2eYTtA9KQgSdyxSBtxHpXF0uQfe0fZqA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:26+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" .
}