@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP319978.RAczYMk_hOvI_etAOVlPk7T9ek1VkGQ0QR08NVlxf63k8
> .
@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#
> .
dgn-np:NP319978.RAczYMk_hOvI_etAOVlPk7T9ek1VkGQ0QR08NVlxf63k8130_head
{
this:
np:hasAssertion
dgn-np:NP319978.RAczYMk_hOvI_etAOVlPk7T9ek1VkGQ0QR08NVlxf63k8130_assertion
;
np:hasProvenance
dgn-np:NP319978.RAczYMk_hOvI_etAOVlPk7T9ek1VkGQ0QR08NVlxf63k8130_provenance
;
np:hasPublicationInfo
dgn-np:NP319978.RAczYMk_hOvI_etAOVlPk7T9ek1VkGQ0QR08NVlxf63k8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP319978.RAczYMk_hOvI_etAOVlPk7T9ek1VkGQ0QR08NVlxf63k8130_assertion
a
np:Assertion
.
dgn-np:NP319978.RAczYMk_hOvI_etAOVlPk7T9ek1VkGQ0QR08NVlxf63k8130_provenance
a
np:Provenance
.
dgn-np:NP319978.RAczYMk_hOvI_etAOVlPk7T9ek1VkGQ0QR08NVlxf63k8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP319978.RAczYMk_hOvI_etAOVlPk7T9ek1VkGQ0QR08NVlxf63k8130_assertion
{
miriam-gene:221458
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNd7f2e6983d45fe7a7effea777781c5fe
sio:SIO_000628
miriam-gene:221458
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP319978.RAczYMk_hOvI_etAOVlPk7T9ek1VkGQ0QR08NVlxf63k8130_provenance
{
dgn-np:NP319978.RAczYMk_hOvI_etAOVlPk7T9ek1VkGQ0QR08NVlxf63k8130_assertion
dcterms:description
"[Additional simulations demonstrated that statin usage, shown in four clinical trials to substantially reduce the excess CHD risk in the KIF6 719Arg variant, should also attenuate the KIF6 719Arg odds ratio in case-control studies.]. 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:21435211
;
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:NP319978.RAczYMk_hOvI_etAOVlPk7T9ek1VkGQ0QR08NVlxf63k8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:05+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" .
}