@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP641061.RAkFcbvgSPWOXTWR-CF6YjCbM1IAVHkZbyclCZ13BoZXg
> .
@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:NP641061.RAkFcbvgSPWOXTWR-CF6YjCbM1IAVHkZbyclCZ13BoZXg130_assertion
;
np:hasProvenance
dgn-np:NP641061.RAkFcbvgSPWOXTWR-CF6YjCbM1IAVHkZbyclCZ13BoZXg130_provenance
;
np:hasPublicationInfo
dgn-np:NP641061.RAkFcbvgSPWOXTWR-CF6YjCbM1IAVHkZbyclCZ13BoZXg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP641061.RAkFcbvgSPWOXTWR-CF6YjCbM1IAVHkZbyclCZ13BoZXg130_assertion
a
np:Assertion
.
dgn-np:NP641061.RAkFcbvgSPWOXTWR-CF6YjCbM1IAVHkZbyclCZ13BoZXg130_provenance
a
np:Provenance
.
dgn-np:NP641061.RAkFcbvgSPWOXTWR-CF6YjCbM1IAVHkZbyclCZ13BoZXg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP641061.RAkFcbvgSPWOXTWR-CF6YjCbM1IAVHkZbyclCZ13BoZXg130_assertion
{
miriam-gene:3106
a
ncit:C16612
.
lld:C0036572
a
ncit:C7057
.
dgn-gda:DGNc109ee03d6230a5b489ae975284269bf
sio:SIO_000628
miriam-gene:3106
,
lld:C0036572
;
a
sio:SIO_001121
.
}
dgn-np:NP641061.RAkFcbvgSPWOXTWR-CF6YjCbM1IAVHkZbyclCZ13BoZXg130_provenance
{
dgn-np:NP641061.RAkFcbvgSPWOXTWR-CF6YjCbM1IAVHkZbyclCZ13BoZXg130_assertion
dcterms:description
"[Although the current studies associating particular genes and their variants with seizure control or adverse events have inherent weaknesses and have not provided unifying conclusions, several results, for example that Asian patients with a particular HLA allele, HLA-B*1502, are at a higher risk for Stevens-Johnson syndrome when using carbamazepine, are helpful to increase our knowledge how genetic variation affects the treatment of epilepsy.]. 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:18627414
;
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:NP641061.RAkFcbvgSPWOXTWR-CF6YjCbM1IAVHkZbyclCZ13BoZXg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
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"v2.1.0" .
}