@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP113162.RACy8Vi_yoMI5Exo4QL5EQDZqsa_hnJ3jqyEKnr2sbfL0
> .
@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/v3.0.0/void/
> .
dgn-np:NP113162.RACy8Vi_yoMI5Exo4QL5EQDZqsa_hnJ3jqyEKnr2sbfL0130_head
{
this:
np:hasAssertion
dgn-np:NP113162.RACy8Vi_yoMI5Exo4QL5EQDZqsa_hnJ3jqyEKnr2sbfL0130_assertion
;
np:hasProvenance
dgn-np:NP113162.RACy8Vi_yoMI5Exo4QL5EQDZqsa_hnJ3jqyEKnr2sbfL0130_provenance
;
np:hasPublicationInfo
dgn-np:NP113162.RACy8Vi_yoMI5Exo4QL5EQDZqsa_hnJ3jqyEKnr2sbfL0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP113162.RACy8Vi_yoMI5Exo4QL5EQDZqsa_hnJ3jqyEKnr2sbfL0130_assertion
a
np:Assertion
.
dgn-np:NP113162.RACy8Vi_yoMI5Exo4QL5EQDZqsa_hnJ3jqyEKnr2sbfL0130_provenance
a
np:Provenance
.
dgn-np:NP113162.RACy8Vi_yoMI5Exo4QL5EQDZqsa_hnJ3jqyEKnr2sbfL0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP113162.RACy8Vi_yoMI5Exo4QL5EQDZqsa_hnJ3jqyEKnr2sbfL0130_assertion
{
miriam-gene:84722
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNc75d07dd1c87d80d7394e9839bf40003
sio:SIO_000628
miriam-gene:84722
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP113162.RACy8Vi_yoMI5Exo4QL5EQDZqsa_hnJ3jqyEKnr2sbfL0130_provenance
{
dgn-np:NP113162.RACy8Vi_yoMI5Exo4QL5EQDZqsa_hnJ3jqyEKnr2sbfL0130_assertion
dcterms:description
"[A genetic risk score based on nine genetic variants independently associated with CAD irrespective of other cardiovascular risk factors was associated with the presence of the disease. Cohort studies are needed to determine whether this genetic risk score]. 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:20738937
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP113162.RACy8Vi_yoMI5Exo4QL5EQDZqsa_hnJ3jqyEKnr2sbfL0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:43+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}