@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP100296.RAq3TFs1A9fT3VldVBQCsKZzuiHmmjfh9KLrNOVPNRkSc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP100296.RAq3TFs1A9fT3VldVBQCsKZzuiHmmjfh9KLrNOVPNRkSc130_head
{
this:
np:hasAssertion
dgn-np:NP100296.RAq3TFs1A9fT3VldVBQCsKZzuiHmmjfh9KLrNOVPNRkSc130_assertion
;
np:hasProvenance
dgn-np:NP100296.RAq3TFs1A9fT3VldVBQCsKZzuiHmmjfh9KLrNOVPNRkSc130_provenance
;
np:hasPublicationInfo
dgn-np:NP100296.RAq3TFs1A9fT3VldVBQCsKZzuiHmmjfh9KLrNOVPNRkSc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP100296.RAq3TFs1A9fT3VldVBQCsKZzuiHmmjfh9KLrNOVPNRkSc130_assertion
a
np:Assertion
.
dgn-np:NP100296.RAq3TFs1A9fT3VldVBQCsKZzuiHmmjfh9KLrNOVPNRkSc130_provenance
a
np:Provenance
.
dgn-np:NP100296.RAq3TFs1A9fT3VldVBQCsKZzuiHmmjfh9KLrNOVPNRkSc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP100296.RAq3TFs1A9fT3VldVBQCsKZzuiHmmjfh9KLrNOVPNRkSc130_assertion
{
miriam-gene:3553
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGNb38df3bba73f00d451eb5f672363456d
sio:SIO_000628
miriam-gene:3553
,
lld:C0004153
;
a
sio:SIO_001122
.
}
dgn-np:NP100296.RAq3TFs1A9fT3VldVBQCsKZzuiHmmjfh9KLrNOVPNRkSc130_provenance
{
dgn-np:NP100296.RAq3TFs1A9fT3VldVBQCsKZzuiHmmjfh9KLrNOVPNRkSc130_assertion
dcterms:description
"[As none of the investigated gene variants was significantly more prevalent in BRVO patients than among control subjects, our data suggest that these polymorphisms themselves are unlikely major risk factors for BRVO.]. 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:19347053
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP100296.RAq3TFs1A9fT3VldVBQCsKZzuiHmmjfh9KLrNOVPNRkSc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:35+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}