@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP772254.RAtAvAaSZH_N9viquqpbKUwIcsZfVux8TEgcoJc6TKvoI
> .
@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:NP772254.RAtAvAaSZH_N9viquqpbKUwIcsZfVux8TEgcoJc6TKvoI130_head
{
this:
np:hasAssertion
dgn-np:NP772254.RAtAvAaSZH_N9viquqpbKUwIcsZfVux8TEgcoJc6TKvoI130_assertion
;
np:hasProvenance
dgn-np:NP772254.RAtAvAaSZH_N9viquqpbKUwIcsZfVux8TEgcoJc6TKvoI130_provenance
;
np:hasPublicationInfo
dgn-np:NP772254.RAtAvAaSZH_N9viquqpbKUwIcsZfVux8TEgcoJc6TKvoI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP772254.RAtAvAaSZH_N9viquqpbKUwIcsZfVux8TEgcoJc6TKvoI130_assertion
a
np:Assertion
.
dgn-np:NP772254.RAtAvAaSZH_N9viquqpbKUwIcsZfVux8TEgcoJc6TKvoI130_provenance
a
np:Provenance
.
dgn-np:NP772254.RAtAvAaSZH_N9viquqpbKUwIcsZfVux8TEgcoJc6TKvoI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP772254.RAtAvAaSZH_N9viquqpbKUwIcsZfVux8TEgcoJc6TKvoI130_assertion
{
miriam-gene:10537
a
ncit:C16612
.
lld:C0014556
a
ncit:C7057
.
dgn-gda:DGNdd325de45a90d4259baf9cdcbb453050
sio:SIO_000628
miriam-gene:10537
,
lld:C0014556
;
a
sio:SIO_001121
.
}
dgn-np:NP772254.RAtAvAaSZH_N9viquqpbKUwIcsZfVux8TEgcoJc6TKvoI130_provenance
{
dgn-np:NP772254.RAtAvAaSZH_N9viquqpbKUwIcsZfVux8TEgcoJc6TKvoI130_assertion
dcterms:description
"[No evidence of significant allelic, genotypic, or haplotypic associations were identified in the tag SNPs of the GABBR1 gene in patients with MTLE, and the polymorphism at G1465A was not observed in our samples.]. 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:18653317
;
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:NP772254.RAtAvAaSZH_N9viquqpbKUwIcsZfVux8TEgcoJc6TKvoI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:47+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" .
}