@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP232110.RA1yd5VPiEXVtHGiMwy2AOVDWFkFIi1RMNv4I6ky5JMbs
> .
@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:NP232110.RA1yd5VPiEXVtHGiMwy2AOVDWFkFIi1RMNv4I6ky5JMbs130_head
{
this:
np:hasAssertion
dgn-np:NP232110.RA1yd5VPiEXVtHGiMwy2AOVDWFkFIi1RMNv4I6ky5JMbs130_assertion
;
np:hasProvenance
dgn-np:NP232110.RA1yd5VPiEXVtHGiMwy2AOVDWFkFIi1RMNv4I6ky5JMbs130_provenance
;
np:hasPublicationInfo
dgn-np:NP232110.RA1yd5VPiEXVtHGiMwy2AOVDWFkFIi1RMNv4I6ky5JMbs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP232110.RA1yd5VPiEXVtHGiMwy2AOVDWFkFIi1RMNv4I6ky5JMbs130_assertion
a
np:Assertion
.
dgn-np:NP232110.RA1yd5VPiEXVtHGiMwy2AOVDWFkFIi1RMNv4I6ky5JMbs130_provenance
a
np:Provenance
.
dgn-np:NP232110.RA1yd5VPiEXVtHGiMwy2AOVDWFkFIi1RMNv4I6ky5JMbs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP232110.RA1yd5VPiEXVtHGiMwy2AOVDWFkFIi1RMNv4I6ky5JMbs130_assertion
{
miriam-gene:8181
a
ncit:C16612
.
lld:C2931469
a
ncit:C7057
.
dgn-gda:DGNcd18f1884e02c6511ab0423aac5b95d3
sio:SIO_000628
miriam-gene:8181
,
lld:C2931469
;
a
sio:SIO_001121
.
}
dgn-np:NP232110.RA1yd5VPiEXVtHGiMwy2AOVDWFkFIi1RMNv4I6ky5JMbs130_provenance
{
dgn-np:NP232110.RA1yd5VPiEXVtHGiMwy2AOVDWFkFIi1RMNv4I6ky5JMbs130_assertion
dcterms:description
"[Susceptibility genes have been localized in five syndromes: autosomal dominant nocturnal frontal lobe epilepsy (20q, 1q, and 15q), autosomal dominant partial epilepsy with auditory features (10q), familial partial epilepsy with variable foci (22q), benign epilepsy of childhood with centrotemporal spikes (15q), and benign familial infantile convulsions (19q).]. 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:11887964
;
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:NP232110.RA1yd5VPiEXVtHGiMwy2AOVDWFkFIi1RMNv4I6ky5JMbs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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" .
}