@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP349362.RA3JeBAcqi77qVu8LfJ7MXLIVC1rM35unvNtijquVsGjo
> .
@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:NP349362.RA3JeBAcqi77qVu8LfJ7MXLIVC1rM35unvNtijquVsGjo130_head
{
this:
np:hasAssertion
dgn-np:NP349362.RA3JeBAcqi77qVu8LfJ7MXLIVC1rM35unvNtijquVsGjo130_assertion
;
np:hasProvenance
dgn-np:NP349362.RA3JeBAcqi77qVu8LfJ7MXLIVC1rM35unvNtijquVsGjo130_provenance
;
np:hasPublicationInfo
dgn-np:NP349362.RA3JeBAcqi77qVu8LfJ7MXLIVC1rM35unvNtijquVsGjo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP349362.RA3JeBAcqi77qVu8LfJ7MXLIVC1rM35unvNtijquVsGjo130_assertion
a
np:Assertion
.
dgn-np:NP349362.RA3JeBAcqi77qVu8LfJ7MXLIVC1rM35unvNtijquVsGjo130_provenance
a
np:Provenance
.
dgn-np:NP349362.RA3JeBAcqi77qVu8LfJ7MXLIVC1rM35unvNtijquVsGjo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP349362.RA3JeBAcqi77qVu8LfJ7MXLIVC1rM35unvNtijquVsGjo130_assertion
{
miriam-gene:2022
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGNfc9ba0b8c0b4535b52083e26cec49202
sio:SIO_000628
miriam-gene:2022
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP349362.RA3JeBAcqi77qVu8LfJ7MXLIVC1rM35unvNtijquVsGjo130_provenance
{
dgn-np:NP349362.RA3JeBAcqi77qVu8LfJ7MXLIVC1rM35unvNtijquVsGjo130_assertion
dcterms:description
"[We tested if sEng would be elevated in brain AVM tissues relative to epilepsy brain tissues, and also investigated whether sEng overexpression via gene transfer in the mouse brain would induce vascular dysplasia and associated changes in downstream signaling pathways.]. 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:19670444
;
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:NP349362.RA3JeBAcqi77qVu8LfJ7MXLIVC1rM35unvNtijquVsGjo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:25+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" .
}