@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP94048.RAAf5h20RHeWGGUH03qO72_aHLPWZkr7ECAjUZVbVGRz8
> .
@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:NP94048.RAAf5h20RHeWGGUH03qO72_aHLPWZkr7ECAjUZVbVGRz8130_head
{
this:
np:hasAssertion
dgn-np:NP94048.RAAf5h20RHeWGGUH03qO72_aHLPWZkr7ECAjUZVbVGRz8130_assertion
;
np:hasProvenance
dgn-np:NP94048.RAAf5h20RHeWGGUH03qO72_aHLPWZkr7ECAjUZVbVGRz8130_provenance
;
np:hasPublicationInfo
dgn-np:NP94048.RAAf5h20RHeWGGUH03qO72_aHLPWZkr7ECAjUZVbVGRz8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP94048.RAAf5h20RHeWGGUH03qO72_aHLPWZkr7ECAjUZVbVGRz8130_assertion
a
np:Assertion
.
dgn-np:NP94048.RAAf5h20RHeWGGUH03qO72_aHLPWZkr7ECAjUZVbVGRz8130_provenance
a
np:Provenance
.
dgn-np:NP94048.RAAf5h20RHeWGGUH03qO72_aHLPWZkr7ECAjUZVbVGRz8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP94048.RAAf5h20RHeWGGUH03qO72_aHLPWZkr7ECAjUZVbVGRz8130_assertion
{
miriam-gene:1761
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGNbfaf5cfb11b53de3daab4a833321764f
sio:SIO_000628
miriam-gene:1761
,
lld:C0007222
;
a
sio:SIO_001122
.
}
dgn-np:NP94048.RAAf5h20RHeWGGUH03qO72_aHLPWZkr7ECAjUZVbVGRz8130_provenance
{
dgn-np:NP94048.RAAf5h20RHeWGGUH03qO72_aHLPWZkr7ECAjUZVbVGRz8130_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:NP94048.RAAf5h20RHeWGGUH03qO72_aHLPWZkr7ECAjUZVbVGRz8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:47+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" .
}