@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA
> .
@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:NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_head
{
this:
np:hasAssertion
dgn-np:NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_assertion
;
np:hasProvenance
dgn-np:NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_provenance
;
np:hasPublicationInfo
dgn-np:NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_assertion
a
np:Assertion
.
dgn-np:NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_provenance
a
np:Provenance
.
dgn-np:NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_assertion
{
miriam-gene:10407
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN1a540259b154e0c0f87b6b8187a40176
sio:SIO_000628
miriam-gene:10407
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_provenance
{
dgn-np:NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_assertion
dcterms:description
"[A functional SNP of the EP2 gene associated with risk of AIA should decrease the transcription level, resulting in reduction of the PGE(2) braking mechanism of inflammation and involvement in the molecular mechanism underlying AIA.]. 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:15496426
;
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:NP181311.RAWFbYjsoiHj4rEQyaP4GhTKY6GQBjMlpeyvpgIc4pghA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}