@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP576635.RAHZ6Rx4NcPKcavgw_aURXSXiV5-Y9nRa-4GaXxhMjjCw
> .
@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:NP576635.RAHZ6Rx4NcPKcavgw_aURXSXiV5-Y9nRa-4GaXxhMjjCw130_head
{
this:
np:hasAssertion
dgn-np:NP576635.RAHZ6Rx4NcPKcavgw_aURXSXiV5-Y9nRa-4GaXxhMjjCw130_assertion
;
np:hasProvenance
dgn-np:NP576635.RAHZ6Rx4NcPKcavgw_aURXSXiV5-Y9nRa-4GaXxhMjjCw130_provenance
;
np:hasPublicationInfo
dgn-np:NP576635.RAHZ6Rx4NcPKcavgw_aURXSXiV5-Y9nRa-4GaXxhMjjCw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP576635.RAHZ6Rx4NcPKcavgw_aURXSXiV5-Y9nRa-4GaXxhMjjCw130_assertion
a
np:Assertion
.
dgn-np:NP576635.RAHZ6Rx4NcPKcavgw_aURXSXiV5-Y9nRa-4GaXxhMjjCw130_provenance
a
np:Provenance
.
dgn-np:NP576635.RAHZ6Rx4NcPKcavgw_aURXSXiV5-Y9nRa-4GaXxhMjjCw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP576635.RAHZ6Rx4NcPKcavgw_aURXSXiV5-Y9nRa-4GaXxhMjjCw130_assertion
{
miriam-gene:4815
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN64ba7220d27cac28f38543b065652968
sio:SIO_000628
miriam-gene:4815
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP576635.RAHZ6Rx4NcPKcavgw_aURXSXiV5-Y9nRa-4GaXxhMjjCw130_provenance
{
dgn-np:NP576635.RAHZ6Rx4NcPKcavgw_aURXSXiV5-Y9nRa-4GaXxhMjjCw130_assertion
dcterms:description
"[Recent genome-wide association (GWA) studies have identified two intergenic single nucleotide polymorphisms (SNPs) (rs11833579 and rs12425791) on chromosome 12p13 and within 11 kb of the NINJ2 gene that were significantly associated with stroke in Caucasians.]. 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:21376321
;
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:NP576635.RAHZ6Rx4NcPKcavgw_aURXSXiV5-Y9nRa-4GaXxhMjjCw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:47+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" .
}