@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP719554.RAtwGQUXCHMSaBAVICh6z4Vb3wVoOB5uASzrqPfqi3kk0
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP719554.RAtwGQUXCHMSaBAVICh6z4Vb3wVoOB5uASzrqPfqi3kk0130_assertion
;
np:hasProvenance
dgn-np:NP719554.RAtwGQUXCHMSaBAVICh6z4Vb3wVoOB5uASzrqPfqi3kk0130_provenance
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np:hasPublicationInfo
dgn-np:NP719554.RAtwGQUXCHMSaBAVICh6z4Vb3wVoOB5uASzrqPfqi3kk0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP719554.RAtwGQUXCHMSaBAVICh6z4Vb3wVoOB5uASzrqPfqi3kk0130_assertion
a
np:Assertion
.
dgn-np:NP719554.RAtwGQUXCHMSaBAVICh6z4Vb3wVoOB5uASzrqPfqi3kk0130_provenance
a
np:Provenance
.
dgn-np:NP719554.RAtwGQUXCHMSaBAVICh6z4Vb3wVoOB5uASzrqPfqi3kk0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP719554.RAtwGQUXCHMSaBAVICh6z4Vb3wVoOB5uASzrqPfqi3kk0130_assertion
{
miriam-gene:828
a
ncit:C16612
.
lld:C0334121
a
ncit:C7057
.
dgn-gda:DGN36e357dc1e2fa54a0c385b3bc7c706e0
sio:SIO_000628
miriam-gene:828
,
lld:C0334121
;
a
sio:SIO_001121
.
}
dgn-np:NP719554.RAtwGQUXCHMSaBAVICh6z4Vb3wVoOB5uASzrqPfqi3kk0130_provenance
{
dgn-np:NP719554.RAtwGQUXCHMSaBAVICh6z4Vb3wVoOB5uASzrqPfqi3kk0130_assertion
dcterms:description
"[In three large community based independent populations (CAPS, KORA and Young Finns) of European ancestry in which common carotid IMT had been measured (total 4961 individuals), we determined whether SNPs that have been associated with CAD in GWAS studies are also associated with carotid IMT.]. 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:21924425
;
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:NP719554.RAtwGQUXCHMSaBAVICh6z4Vb3wVoOB5uASzrqPfqi3kk0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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
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"v2.1.0" .
}