@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP66724.RAg4xZmE28NPeHdMlCKoyRLXalervELOquLD0LqYQ5-Ds
> .
@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:NP66724.RAg4xZmE28NPeHdMlCKoyRLXalervELOquLD0LqYQ5-Ds130_head
{
this:
np:hasAssertion
dgn-np:NP66724.RAg4xZmE28NPeHdMlCKoyRLXalervELOquLD0LqYQ5-Ds130_assertion
;
np:hasProvenance
dgn-np:NP66724.RAg4xZmE28NPeHdMlCKoyRLXalervELOquLD0LqYQ5-Ds130_provenance
;
np:hasPublicationInfo
dgn-np:NP66724.RAg4xZmE28NPeHdMlCKoyRLXalervELOquLD0LqYQ5-Ds130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP66724.RAg4xZmE28NPeHdMlCKoyRLXalervELOquLD0LqYQ5-Ds130_assertion
a
np:Assertion
.
dgn-np:NP66724.RAg4xZmE28NPeHdMlCKoyRLXalervELOquLD0LqYQ5-Ds130_provenance
a
np:Provenance
.
dgn-np:NP66724.RAg4xZmE28NPeHdMlCKoyRLXalervELOquLD0LqYQ5-Ds130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP66724.RAg4xZmE28NPeHdMlCKoyRLXalervELOquLD0LqYQ5-Ds130_assertion
{
miriam-gene:5144
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN2a2fd1051d3566795acaa275b6d2a48e
sio:SIO_000628
miriam-gene:5144
,
lld:C0038454
;
a
sio:SIO_001122
.
}
dgn-np:NP66724.RAg4xZmE28NPeHdMlCKoyRLXalervELOquLD0LqYQ5-Ds130_provenance
{
dgn-np:NP66724.RAg4xZmE28NPeHdMlCKoyRLXalervELOquLD0LqYQ5-Ds130_assertion
dcterms:description
"[The ALOX5AP SG13S114 variant is an independent risk factor for IS in the Iberian population and is associated with ALOX5AP expression levels. The role of this gene in stroke merits further investigation.]. 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:20357438
;
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:NP66724.RAg4xZmE28NPeHdMlCKoyRLXalervELOquLD0LqYQ5-Ds130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:16+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" .
}