@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP721169.RAZyWKymHkr-8c7DTM6siVq9TmHEGM20GcVWQjKQvBfig
> .
@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:NP721169.RAZyWKymHkr-8c7DTM6siVq9TmHEGM20GcVWQjKQvBfig130_head
{
this:
np:hasAssertion
dgn-np:NP721169.RAZyWKymHkr-8c7DTM6siVq9TmHEGM20GcVWQjKQvBfig130_assertion
;
np:hasProvenance
dgn-np:NP721169.RAZyWKymHkr-8c7DTM6siVq9TmHEGM20GcVWQjKQvBfig130_provenance
;
np:hasPublicationInfo
dgn-np:NP721169.RAZyWKymHkr-8c7DTM6siVq9TmHEGM20GcVWQjKQvBfig130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP721169.RAZyWKymHkr-8c7DTM6siVq9TmHEGM20GcVWQjKQvBfig130_assertion
a
np:Assertion
.
dgn-np:NP721169.RAZyWKymHkr-8c7DTM6siVq9TmHEGM20GcVWQjKQvBfig130_provenance
a
np:Provenance
.
dgn-np:NP721169.RAZyWKymHkr-8c7DTM6siVq9TmHEGM20GcVWQjKQvBfig130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP721169.RAZyWKymHkr-8c7DTM6siVq9TmHEGM20GcVWQjKQvBfig130_assertion
{
miriam-gene:2703
a
ncit:C16612
.
lld:C0027066
a
ncit:C7057
.
dgn-gda:DGN097e1ea251069319e78aa53f9f7cc2fc
sio:SIO_000628
miriam-gene:2703
,
lld:C0027066
;
a
sio:SIO_001121
.
}
dgn-np:NP721169.RAZyWKymHkr-8c7DTM6siVq9TmHEGM20GcVWQjKQvBfig130_provenance
{
dgn-np:NP721169.RAZyWKymHkr-8c7DTM6siVq9TmHEGM20GcVWQjKQvBfig130_assertion
dcterms:description
"[Among the 129 patients with absences without significant myoclonus, 50 had juvenile absence epilepsy 44 had CAE according to the CAE 1989 criteria and only 30 had CAE according to the CAE 2005 criteria.]. 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:17666074
;
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:NP721169.RAZyWKymHkr-8c7DTM6siVq9TmHEGM20GcVWQjKQvBfig130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:18+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" .
}