@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563682.RAo_SGzm8YfMy2zpDahWMkHl1SWsptsVu98bPAdgvP8Qg
> .
@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:NP563682.RAo_SGzm8YfMy2zpDahWMkHl1SWsptsVu98bPAdgvP8Qg130_head
{
this:
np:hasAssertion
dgn-np:NP563682.RAo_SGzm8YfMy2zpDahWMkHl1SWsptsVu98bPAdgvP8Qg130_assertion
;
np:hasProvenance
dgn-np:NP563682.RAo_SGzm8YfMy2zpDahWMkHl1SWsptsVu98bPAdgvP8Qg130_provenance
;
np:hasPublicationInfo
dgn-np:NP563682.RAo_SGzm8YfMy2zpDahWMkHl1SWsptsVu98bPAdgvP8Qg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563682.RAo_SGzm8YfMy2zpDahWMkHl1SWsptsVu98bPAdgvP8Qg130_assertion
a
np:Assertion
.
dgn-np:NP563682.RAo_SGzm8YfMy2zpDahWMkHl1SWsptsVu98bPAdgvP8Qg130_provenance
a
np:Provenance
.
dgn-np:NP563682.RAo_SGzm8YfMy2zpDahWMkHl1SWsptsVu98bPAdgvP8Qg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP563682.RAo_SGzm8YfMy2zpDahWMkHl1SWsptsVu98bPAdgvP8Qg130_assertion
{
miriam-gene:4899
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN7008684f463273e8295b4e0a84b01d56
sio:SIO_000628
miriam-gene:4899
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP563682.RAo_SGzm8YfMy2zpDahWMkHl1SWsptsVu98bPAdgvP8Qg130_provenance
{
dgn-np:NP563682.RAo_SGzm8YfMy2zpDahWMkHl1SWsptsVu98bPAdgvP8Qg130_assertion
dcterms:description
"[The Evaluation of Genomic Applications in Practice and Prevention Working Group (EWG) found insufficient evidence to recommend testing for the 9p21 genetic variant or 57 other variants in 28 genes (listed in ) to assess risk for cardiovascular disease (CVD) in the general population, specifically heart disease and stroke.]. 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:21042222
;
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:NP563682.RAo_SGzm8YfMy2zpDahWMkHl1SWsptsVu98bPAdgvP8Qg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}