@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP872432.RAGRhQ0LLdwEm5DzBxvEkD1rla67JHyU2G57KOS1tqpcc
> .
@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:NP872432.RAGRhQ0LLdwEm5DzBxvEkD1rla67JHyU2G57KOS1tqpcc130_head
{
this:
np:hasAssertion
dgn-np:NP872432.RAGRhQ0LLdwEm5DzBxvEkD1rla67JHyU2G57KOS1tqpcc130_assertion
;
np:hasProvenance
dgn-np:NP872432.RAGRhQ0LLdwEm5DzBxvEkD1rla67JHyU2G57KOS1tqpcc130_provenance
;
np:hasPublicationInfo
dgn-np:NP872432.RAGRhQ0LLdwEm5DzBxvEkD1rla67JHyU2G57KOS1tqpcc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP872432.RAGRhQ0LLdwEm5DzBxvEkD1rla67JHyU2G57KOS1tqpcc130_assertion
a
np:Assertion
.
dgn-np:NP872432.RAGRhQ0LLdwEm5DzBxvEkD1rla67JHyU2G57KOS1tqpcc130_provenance
a
np:Provenance
.
dgn-np:NP872432.RAGRhQ0LLdwEm5DzBxvEkD1rla67JHyU2G57KOS1tqpcc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP872432.RAGRhQ0LLdwEm5DzBxvEkD1rla67JHyU2G57KOS1tqpcc130_assertion
{
miriam-gene:57526
a
ncit:C16612
.
lld:C0036572
a
ncit:C7057
.
dgn-gda:DGN8bbf8e5e385f5ab58d64919b08b43393
sio:SIO_000628
miriam-gene:57526
,
lld:C0036572
;
a
sio:SIO_001121
.
}
dgn-np:NP872432.RAGRhQ0LLdwEm5DzBxvEkD1rla67JHyU2G57KOS1tqpcc130_provenance
{
dgn-np:NP872432.RAGRhQ0LLdwEm5DzBxvEkD1rla67JHyU2G57KOS1tqpcc130_assertion
dcterms:description
"[Review of clinical data of all reported patients showed that the clinical picture of EFMR is heterogeneous, but epilepsy onset in infancy, fever sensitivity and occurrence of seizures in clusters are key features.]. 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:23334464
;
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:NP872432.RAGRhQ0LLdwEm5DzBxvEkD1rla67JHyU2G57KOS1tqpcc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:53+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" .
}