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http://rdf.disgenet.org/nanopublications.trig#NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg
> .
@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:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_assertion
a
np:Assertion
.
dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_provenance
a
np:Provenance
.
dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:3949
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN69a8aef5fd131ea28bf5e0f9471ba2d1
sio:SIO_000628
miriam-gene:3949
,
lld:C1956346
;
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.
}
dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_provenance
{
dgn-np:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_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 can improve the predictive capacity or the risk classification of classical risk functions.]. 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-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP63267.RAehQn4S0nN6wq1yHJ8q4tsBUQrsiy12zKXSZnYk3vheg130_publicationInfo
{
this:
dcterms:created
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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
<
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> , <
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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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"v2.1.0" .
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