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> .
@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:NP448255.RA63mV611GuVXKVDZGC3E4OLjbYITSrGvp2SWSTr3zeng130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP448255.RA63mV611GuVXKVDZGC3E4OLjbYITSrGvp2SWSTr3zeng130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP448255.RA63mV611GuVXKVDZGC3E4OLjbYITSrGvp2SWSTr3zeng130_provenance
a
np:Provenance
.
dgn-np:NP448255.RA63mV611GuVXKVDZGC3E4OLjbYITSrGvp2SWSTr3zeng130_publicationInfo
a
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.
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{
miriam-gene:404677
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNd2d1d8522d9c10044d9d8d2676a06013
sio:SIO_000628
miriam-gene:404677
,
lld:C1956346
;
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sio:SIO_001121
.
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dgn-np:NP448255.RA63mV611GuVXKVDZGC3E4OLjbYITSrGvp2SWSTr3zeng130_provenance
{
dgn-np:NP448255.RA63mV611GuVXKVDZGC3E4OLjbYITSrGvp2SWSTr3zeng130_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
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;
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 .
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dgn-np:NP448255.RA63mV611GuVXKVDZGC3E4OLjbYITSrGvp2SWSTr3zeng130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:27+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
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pav:authoredBy
<
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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