@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_head
{
this:
np:hasAssertion
dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_assertion
;
np:hasProvenance
dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_provenance
;
np:hasPublicationInfo
dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_assertion
a
np:Assertion
.
dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_provenance
a
np:Provenance
.
dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_assertion
{
miriam-gene:2914
a
ncit:C16612
.
lld:C0014553
a
ncit:C7057
.
dgn-gda:DGN3b70a82a751ccc85966d2bf3ef96cfbb
sio:SIO_000628
miriam-gene:2914
,
lld:C0014553
;
a
sio:SIO_001122
.
}
dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_provenance
{
dgn-np:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_assertion
dcterms:description
"[Association analysis was carried out for 17 single nucleotide polymorphisms (SNPs) covering the genomic GRM4 sequence for all IGE patients as well as for two common IGE subsyndromes Juvenile Myoclonic Epilepsy (JME, n=215) and Childhood Absence Epilepsy (CAE, n=175).]. 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:20338729
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:03+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}