@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP601520.RASX_wJ7bhELUZjTYvHcdm2NN_7qTCFcq4oUOAKBxqpkA
> .
@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:NP601520.RASX_wJ7bhELUZjTYvHcdm2NN_7qTCFcq4oUOAKBxqpkA130_assertion
;
np:hasProvenance
dgn-np:NP601520.RASX_wJ7bhELUZjTYvHcdm2NN_7qTCFcq4oUOAKBxqpkA130_provenance
;
np:hasPublicationInfo
dgn-np:NP601520.RASX_wJ7bhELUZjTYvHcdm2NN_7qTCFcq4oUOAKBxqpkA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601520.RASX_wJ7bhELUZjTYvHcdm2NN_7qTCFcq4oUOAKBxqpkA130_assertion
a
np:Assertion
.
dgn-np:NP601520.RASX_wJ7bhELUZjTYvHcdm2NN_7qTCFcq4oUOAKBxqpkA130_provenance
a
np:Provenance
.
dgn-np:NP601520.RASX_wJ7bhELUZjTYvHcdm2NN_7qTCFcq4oUOAKBxqpkA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601520.RASX_wJ7bhELUZjTYvHcdm2NN_7qTCFcq4oUOAKBxqpkA130_assertion
{
miriam-gene:404677
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNeb47e04c464a831739a45a9604ac60c7
sio:SIO_000628
miriam-gene:404677
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP601520.RASX_wJ7bhELUZjTYvHcdm2NN_7qTCFcq4oUOAKBxqpkA130_provenance
{
dgn-np:NP601520.RASX_wJ7bhELUZjTYvHcdm2NN_7qTCFcq4oUOAKBxqpkA130_assertion
dcterms:description
"[We genotyped 2277 individuals, age 24 to 39 years, from the Cardiovascular Risk in Young Finns Study with CIMT and FMD measurements and 1295 individuals, age 46 to 76 years, from the Health 2000 Survey with CIMT for rs1333049, the chromosome 9p21 variant showing the strongest association with 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:18599798
;
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:NP601520.RASX_wJ7bhELUZjTYvHcdm2NN_7qTCFcq4oUOAKBxqpkA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}