@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177013.RA6xk9HAhjWF9Bl4-OeF7TkioNNz_8OIhm_NMFyjz6bAk
> .
@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:NP177013.RA6xk9HAhjWF9Bl4-OeF7TkioNNz_8OIhm_NMFyjz6bAk130_head
{
this:
np:hasAssertion
dgn-np:NP177013.RA6xk9HAhjWF9Bl4-OeF7TkioNNz_8OIhm_NMFyjz6bAk130_assertion
;
np:hasProvenance
dgn-np:NP177013.RA6xk9HAhjWF9Bl4-OeF7TkioNNz_8OIhm_NMFyjz6bAk130_provenance
;
np:hasPublicationInfo
dgn-np:NP177013.RA6xk9HAhjWF9Bl4-OeF7TkioNNz_8OIhm_NMFyjz6bAk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177013.RA6xk9HAhjWF9Bl4-OeF7TkioNNz_8OIhm_NMFyjz6bAk130_assertion
a
np:Assertion
.
dgn-np:NP177013.RA6xk9HAhjWF9Bl4-OeF7TkioNNz_8OIhm_NMFyjz6bAk130_provenance
a
np:Provenance
.
dgn-np:NP177013.RA6xk9HAhjWF9Bl4-OeF7TkioNNz_8OIhm_NMFyjz6bAk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177013.RA6xk9HAhjWF9Bl4-OeF7TkioNNz_8OIhm_NMFyjz6bAk130_assertion
{
miriam-gene:597
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN229755c03924f8aec6ae2a6ca89d34ad
sio:SIO_000628
miriam-gene:597
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP177013.RA6xk9HAhjWF9Bl4-OeF7TkioNNz_8OIhm_NMFyjz6bAk130_provenance
{
dgn-np:NP177013.RA6xk9HAhjWF9Bl4-OeF7TkioNNz_8OIhm_NMFyjz6bAk130_assertion
dcterms:description
"[A GRS composed of 13 SNPs associated with coronary disease is an independent predictor of cardiovascular events and of high CAC, modestly improves risk reclassification for incident CHD, and significantly improves discrimination for high CAC.]. 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:22235037
;
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:NP177013.RA6xk9HAhjWF9Bl4-OeF7TkioNNz_8OIhm_NMFyjz6bAk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:35+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" .
}