@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP567311.RA0_jtn_fPmFoM0158m-qyJFbS8PZx3pa3nRR7NWy4oUk
> .
@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:NP567311.RA0_jtn_fPmFoM0158m-qyJFbS8PZx3pa3nRR7NWy4oUk130_assertion
;
np:hasProvenance
dgn-np:NP567311.RA0_jtn_fPmFoM0158m-qyJFbS8PZx3pa3nRR7NWy4oUk130_provenance
;
np:hasPublicationInfo
dgn-np:NP567311.RA0_jtn_fPmFoM0158m-qyJFbS8PZx3pa3nRR7NWy4oUk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP567311.RA0_jtn_fPmFoM0158m-qyJFbS8PZx3pa3nRR7NWy4oUk130_assertion
a
np:Assertion
.
dgn-np:NP567311.RA0_jtn_fPmFoM0158m-qyJFbS8PZx3pa3nRR7NWy4oUk130_provenance
a
np:Provenance
.
dgn-np:NP567311.RA0_jtn_fPmFoM0158m-qyJFbS8PZx3pa3nRR7NWy4oUk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP567311.RA0_jtn_fPmFoM0158m-qyJFbS8PZx3pa3nRR7NWy4oUk130_assertion
{
miriam-gene:6950
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN62bb4964bfa9fd9ad11150ee94779afa
sio:SIO_000628
miriam-gene:6950
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP567311.RA0_jtn_fPmFoM0158m-qyJFbS8PZx3pa3nRR7NWy4oUk130_provenance
{
dgn-np:NP567311.RA0_jtn_fPmFoM0158m-qyJFbS8PZx3pa3nRR7NWy4oUk130_assertion
dcterms:description
"[The objectives of the present study were to assess the prevalence and magnitude of subclinical CAD in patients with HeFH using coronary computed tomographic angiography (CCTA) and to determine the clinical and genetic profile of those at the greatest risk of CAD.]. 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:23340035
;
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:NP567311.RA0_jtn_fPmFoM0158m-qyJFbS8PZx3pa3nRR7NWy4oUk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:42+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
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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
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"v2.1.0" .
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