@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU
> .
@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:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_head
{
this:
np:hasAssertion
dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_assertion
;
np:hasProvenance
dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_provenance
;
np:hasPublicationInfo
dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_assertion
a
np:Assertion
.
dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_provenance
a
np:Provenance
.
dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_assertion
{
miriam-gene:50987
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGNb77178bad36cfd7d37bd3f60dec67dda
sio:SIO_000628
miriam-gene:50987
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_provenance
{
dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_assertion
dcterms:description
"[Familial partial epilepsy with variable foci (FPEVF) is an autosomal dominant form of partial epilepsy characterized by the presence of epileptic seizures originating from different cerebral lobes in different members of the same family.]. 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:20659149
;
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:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:00+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" .
}