@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP793537.RA980_NAccxNZjO9ZALZofHmt8ylVcNzn1RVWH3NE0Obw
> .
@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:NP793537.RA980_NAccxNZjO9ZALZofHmt8ylVcNzn1RVWH3NE0Obw130_head
{
this:
np:hasAssertion
dgn-np:NP793537.RA980_NAccxNZjO9ZALZofHmt8ylVcNzn1RVWH3NE0Obw130_assertion
;
np:hasProvenance
dgn-np:NP793537.RA980_NAccxNZjO9ZALZofHmt8ylVcNzn1RVWH3NE0Obw130_provenance
;
np:hasPublicationInfo
dgn-np:NP793537.RA980_NAccxNZjO9ZALZofHmt8ylVcNzn1RVWH3NE0Obw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP793537.RA980_NAccxNZjO9ZALZofHmt8ylVcNzn1RVWH3NE0Obw130_assertion
a
np:Assertion
.
dgn-np:NP793537.RA980_NAccxNZjO9ZALZofHmt8ylVcNzn1RVWH3NE0Obw130_provenance
a
np:Provenance
.
dgn-np:NP793537.RA980_NAccxNZjO9ZALZofHmt8ylVcNzn1RVWH3NE0Obw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP793537.RA980_NAccxNZjO9ZALZofHmt8ylVcNzn1RVWH3NE0Obw130_assertion
{
miriam-gene:170302
a
ncit:C16612
.
lld:C0543888
a
ncit:C7057
.
dgn-gda:DGNc26e126d9e589f22f5b61e4ffee04e42
sio:SIO_000628
miriam-gene:170302
,
lld:C0543888
;
a
sio:SIO_001121
.
}
dgn-np:NP793537.RA980_NAccxNZjO9ZALZofHmt8ylVcNzn1RVWH3NE0Obw130_provenance
{
dgn-np:NP793537.RA980_NAccxNZjO9ZALZofHmt8ylVcNzn1RVWH3NE0Obw130_assertion
dcterms:description
"[Our findings confirm the role of ARX in the pathogenesis of early epilepsy and underline the importance of screening of the ARX gene in both male and female subjects with otherwise unexplained early onset epileptic encephalopathy.]. 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:23039062
;
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 .
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dgn-np:NP793537.RA980_NAccxNZjO9ZALZofHmt8ylVcNzn1RVWH3NE0Obw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:07+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" .
}