@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP99866.RAYNcofmNJITMZzjz3bdOw9Qp9VtqOpAD_Lo5TWj9rCVw
> .
@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:NP99866.RAYNcofmNJITMZzjz3bdOw9Qp9VtqOpAD_Lo5TWj9rCVw130_head
{
this:
np:hasAssertion
dgn-np:NP99866.RAYNcofmNJITMZzjz3bdOw9Qp9VtqOpAD_Lo5TWj9rCVw130_assertion
;
np:hasProvenance
dgn-np:NP99866.RAYNcofmNJITMZzjz3bdOw9Qp9VtqOpAD_Lo5TWj9rCVw130_provenance
;
np:hasPublicationInfo
dgn-np:NP99866.RAYNcofmNJITMZzjz3bdOw9Qp9VtqOpAD_Lo5TWj9rCVw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP99866.RAYNcofmNJITMZzjz3bdOw9Qp9VtqOpAD_Lo5TWj9rCVw130_assertion
a
np:Assertion
.
dgn-np:NP99866.RAYNcofmNJITMZzjz3bdOw9Qp9VtqOpAD_Lo5TWj9rCVw130_provenance
a
np:Provenance
.
dgn-np:NP99866.RAYNcofmNJITMZzjz3bdOw9Qp9VtqOpAD_Lo5TWj9rCVw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP99866.RAYNcofmNJITMZzjz3bdOw9Qp9VtqOpAD_Lo5TWj9rCVw130_assertion
{
miriam-gene:3557
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN8e9da99c2cfe06995d981bcdb7a31550
sio:SIO_000628
miriam-gene:3557
,
lld:C0038454
;
a
sio:SIO_001122
.
}
dgn-np:NP99866.RAYNcofmNJITMZzjz3bdOw9Qp9VtqOpAD_Lo5TWj9rCVw130_provenance
{
dgn-np:NP99866.RAYNcofmNJITMZzjz3bdOw9Qp9VtqOpAD_Lo5TWj9rCVw130_assertion
dcterms:description
"[These results suggest that IL1RN*1/IL1RN*2 genotype in greater Yin person might be associated with increased risk of ischemic stroke, and rs7535475 of FCGR2A might be associated with decreased risk of ischemic stroke. Furthermore, this relationship could ]. 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:20034444
;
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:NP99866.RAYNcofmNJITMZzjz3bdOw9Qp9VtqOpAD_Lo5TWj9rCVw130_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" .
}