@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP518308.RA2nWkxXGemgtQ87PJPUs33deqfKNpBagoTLGGk1J67bw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP518308.RA2nWkxXGemgtQ87PJPUs33deqfKNpBagoTLGGk1J67bw130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP518308.RA2nWkxXGemgtQ87PJPUs33deqfKNpBagoTLGGk1J67bw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP518308.RA2nWkxXGemgtQ87PJPUs33deqfKNpBagoTLGGk1J67bw130_assertion
a
np:Assertion
.
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a
np:Provenance
.
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{
miriam-gene:3075
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGN15ebe66fdd7a9186b1632a60f4e4f5e0
sio:SIO_000628
miriam-gene:3075
,
lld:C0040038
;
a
sio:SIO_001122
.
}
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{
dgn-np:NP518308.RA2nWkxXGemgtQ87PJPUs33deqfKNpBagoTLGGk1J67bw130_assertion
dcterms:description
"[We, therefore, evaluated the CFH genetic variant Y402H amongst 685 Caucasian individuals who subsequently developed arterial or venous thrombotic event (incident myocardial infarction (MI), ischaemic stroke, or venous thromboembolism) and amongst 685 age- and smoking-matched Caucasian individuals who remained free of reported vascular disease during follow-up (controls) within the Physicians' Health Study cohort.]. 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:16229850
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP518308.RA2nWkxXGemgtQ87PJPUs33deqfKNpBagoTLGGk1J67bw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:39+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
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;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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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
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"v4.0.0" .
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