@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k
> .
@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:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_head
{
this:
np:hasAssertion
dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_assertion
;
np:hasProvenance
dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_provenance
;
np:hasPublicationInfo
dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_assertion
a
np:Assertion
.
dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_provenance
a
np:Provenance
.
dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_assertion
{
miriam-gene:116519
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN5864b27ef83ce0bd17eb7c8869d81687
sio:SIO_000628
miriam-gene:116519
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_provenance
{
dgn-np:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_assertion
dcterms:description
"[Multiplex regression analysis model adjusted for age, gender, serum total cholesterol levels, acute myocardial infarction and stroke events revealed that the examined ApoA5 variant confers risk for the development of metabolic syndrome: the odds ratio at 95% confidence interval was 3.622 (1.200-10.936), p=0.02.]. 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:17922054
;
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:NP741924.RAo-QADFJJPtkRFn4t0iAKIbG1ifBb_CKoBu3ZIkn453k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:30+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" .
}