@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP50220.RAdpJsZGVcefEknJq7m187vLplULuoXEhTmqWvfWXWBdM
> .
@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:NP50220.RAdpJsZGVcefEknJq7m187vLplULuoXEhTmqWvfWXWBdM130_head
{
this:
np:hasAssertion
dgn-np:NP50220.RAdpJsZGVcefEknJq7m187vLplULuoXEhTmqWvfWXWBdM130_assertion
;
np:hasProvenance
dgn-np:NP50220.RAdpJsZGVcefEknJq7m187vLplULuoXEhTmqWvfWXWBdM130_provenance
;
np:hasPublicationInfo
dgn-np:NP50220.RAdpJsZGVcefEknJq7m187vLplULuoXEhTmqWvfWXWBdM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50220.RAdpJsZGVcefEknJq7m187vLplULuoXEhTmqWvfWXWBdM130_assertion
a
np:Assertion
.
dgn-np:NP50220.RAdpJsZGVcefEknJq7m187vLplULuoXEhTmqWvfWXWBdM130_provenance
a
np:Provenance
.
dgn-np:NP50220.RAdpJsZGVcefEknJq7m187vLplULuoXEhTmqWvfWXWBdM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50220.RAdpJsZGVcefEknJq7m187vLplULuoXEhTmqWvfWXWBdM130_assertion
{
miriam-gene:7124
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGNa1dd04b7cc146b77520b5ee579171340
sio:SIO_000628
miriam-gene:7124
,
lld:C0010054
;
a
sio:SIO_001122
.
}
dgn-np:NP50220.RAdpJsZGVcefEknJq7m187vLplULuoXEhTmqWvfWXWBdM130_provenance
{
dgn-np:NP50220.RAdpJsZGVcefEknJq7m187vLplULuoXEhTmqWvfWXWBdM130_assertion
dcterms:description
"[ The association of APOE, DRB1, D6589 and TNFa alleles with risk of CHD suggest that these are candidate genes or linked to genes for CHD in this cohort of AAW. Our data supported elevated plasma Lp(a) as a potential risk factor in AAW; however, its role is still unclear. The premenopausal AAW in this sample had a higher than expected rate of metabolic syndrome, which was associated with DRB1 alleles.]. 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:15825968
;
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:NP50220.RAdpJsZGVcefEknJq7m187vLplULuoXEhTmqWvfWXWBdM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}