@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP55809.RA4afHcPuLlSmWZmOIlm3NYB22LEJEKp8KioblyX9CHrY
> .
@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 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:NP55809.RA4afHcPuLlSmWZmOIlm3NYB22LEJEKp8KioblyX9CHrY130_head
{
this:
np:hasAssertion
dgn-np:NP55809.RA4afHcPuLlSmWZmOIlm3NYB22LEJEKp8KioblyX9CHrY130_assertion
;
np:hasProvenance
dgn-np:NP55809.RA4afHcPuLlSmWZmOIlm3NYB22LEJEKp8KioblyX9CHrY130_provenance
;
np:hasPublicationInfo
dgn-np:NP55809.RA4afHcPuLlSmWZmOIlm3NYB22LEJEKp8KioblyX9CHrY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55809.RA4afHcPuLlSmWZmOIlm3NYB22LEJEKp8KioblyX9CHrY130_assertion
a
np:Assertion
.
dgn-np:NP55809.RA4afHcPuLlSmWZmOIlm3NYB22LEJEKp8KioblyX9CHrY130_provenance
a
np:Provenance
.
dgn-np:NP55809.RA4afHcPuLlSmWZmOIlm3NYB22LEJEKp8KioblyX9CHrY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55809.RA4afHcPuLlSmWZmOIlm3NYB22LEJEKp8KioblyX9CHrY130_assertion
{
miriam-gene:3667
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN8cc80633d0ef37c92934c014b5f2affb
sio:SIO_000628
miriam-gene:3667
,
lld:C0007222
;
a
sio:SIO_001122
.
}
dgn-np:NP55809.RA4afHcPuLlSmWZmOIlm3NYB22LEJEKp8KioblyX9CHrY130_provenance
{
dgn-np:NP55809.RA4afHcPuLlSmWZmOIlm3NYB22LEJEKp8KioblyX9CHrY130_assertion
dcterms:description
"[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. 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:17903304
;
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 .
}
dgn-np:NP55809.RA4afHcPuLlSmWZmOIlm3NYB22LEJEKp8KioblyX9CHrY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:26+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
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}