@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP878230.RAB9szihaBUSgYj-dtoVuPZ887zJPWhHtLZN1eHkrpw3c
> .
@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:NP878230.RAB9szihaBUSgYj-dtoVuPZ887zJPWhHtLZN1eHkrpw3c130_head
{
this:
np:hasAssertion
dgn-np:NP878230.RAB9szihaBUSgYj-dtoVuPZ887zJPWhHtLZN1eHkrpw3c130_assertion
;
np:hasProvenance
dgn-np:NP878230.RAB9szihaBUSgYj-dtoVuPZ887zJPWhHtLZN1eHkrpw3c130_provenance
;
np:hasPublicationInfo
dgn-np:NP878230.RAB9szihaBUSgYj-dtoVuPZ887zJPWhHtLZN1eHkrpw3c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP878230.RAB9szihaBUSgYj-dtoVuPZ887zJPWhHtLZN1eHkrpw3c130_assertion
a
np:Assertion
.
dgn-np:NP878230.RAB9szihaBUSgYj-dtoVuPZ887zJPWhHtLZN1eHkrpw3c130_provenance
a
np:Provenance
.
dgn-np:NP878230.RAB9szihaBUSgYj-dtoVuPZ887zJPWhHtLZN1eHkrpw3c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP878230.RAB9szihaBUSgYj-dtoVuPZ887zJPWhHtLZN1eHkrpw3c130_assertion
{
miriam-gene:50987
a
ncit:C16612
.
lld:C0014547
a
ncit:C7057
.
dgn-gda:DGN7ec271a84ed36c77fccf0569cd918ccd
sio:SIO_000628
miriam-gene:50987
,
lld:C0014547
;
a
sio:SIO_001121
.
}
dgn-np:NP878230.RAB9szihaBUSgYj-dtoVuPZ887zJPWhHtLZN1eHkrpw3c130_provenance
{
dgn-np:NP878230.RAB9szihaBUSgYj-dtoVuPZ887zJPWhHtLZN1eHkrpw3c130_assertion
dcterms:description
"[Familial partial epilepsy with variable foci (FPEVF) is an autosomal dominant syndrome characterized by partial seizures originating from different brain regions in different family members in the absence of detectable structural abnormalities.]. 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:15329069
;
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:NP878230.RAB9szihaBUSgYj-dtoVuPZ887zJPWhHtLZN1eHkrpw3c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:56+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" .
}