@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP809292.RAjnsfI4iGLXdcQN4m8_K2girkef4gz6-3y2RgopuhVCY
> .
@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:NP809292.RAjnsfI4iGLXdcQN4m8_K2girkef4gz6-3y2RgopuhVCY130_head
{
this:
np:hasAssertion
dgn-np:NP809292.RAjnsfI4iGLXdcQN4m8_K2girkef4gz6-3y2RgopuhVCY130_assertion
;
np:hasProvenance
dgn-np:NP809292.RAjnsfI4iGLXdcQN4m8_K2girkef4gz6-3y2RgopuhVCY130_provenance
;
np:hasPublicationInfo
dgn-np:NP809292.RAjnsfI4iGLXdcQN4m8_K2girkef4gz6-3y2RgopuhVCY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP809292.RAjnsfI4iGLXdcQN4m8_K2girkef4gz6-3y2RgopuhVCY130_assertion
a
np:Assertion
.
dgn-np:NP809292.RAjnsfI4iGLXdcQN4m8_K2girkef4gz6-3y2RgopuhVCY130_provenance
a
np:Provenance
.
dgn-np:NP809292.RAjnsfI4iGLXdcQN4m8_K2girkef4gz6-3y2RgopuhVCY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP809292.RAjnsfI4iGLXdcQN4m8_K2girkef4gz6-3y2RgopuhVCY130_assertion
{
miriam-gene:3785
a
ncit:C16612
.
lld:C0270853
a
ncit:C7057
.
dgn-gda:DGNe027a333823166b9055a8077395dda8f
sio:SIO_000628
miriam-gene:3785
,
lld:C0270853
;
a
sio:SIO_001121
.
}
dgn-np:NP809292.RAjnsfI4iGLXdcQN4m8_K2girkef4gz6-3y2RgopuhVCY130_provenance
{
dgn-np:NP809292.RAjnsfI4iGLXdcQN4m8_K2girkef4gz6-3y2RgopuhVCY130_assertion
dcterms:description
"[Susceptibility genes for two syndromes of idiopathic generalized epilepsies, the benign familial neonatal convulsions and juvenile myoclonic epilepsy, have been assigned to the chromosomal regions 20q13 (EBN1), 8q24 (EBN2) and 6p21 (EJM1).]. 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:8796880
;
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:NP809292.RAjnsfI4iGLXdcQN4m8_K2girkef4gz6-3y2RgopuhVCY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}