@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP407080.RAm01u8TIP-CZT3DRhrvsku4HboeE3Oe2I8w4_SlmJf0c
> .
@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:NP407080.RAm01u8TIP-CZT3DRhrvsku4HboeE3Oe2I8w4_SlmJf0c130_head
{
this:
np:hasAssertion
dgn-np:NP407080.RAm01u8TIP-CZT3DRhrvsku4HboeE3Oe2I8w4_SlmJf0c130_assertion
;
np:hasProvenance
dgn-np:NP407080.RAm01u8TIP-CZT3DRhrvsku4HboeE3Oe2I8w4_SlmJf0c130_provenance
;
np:hasPublicationInfo
dgn-np:NP407080.RAm01u8TIP-CZT3DRhrvsku4HboeE3Oe2I8w4_SlmJf0c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP407080.RAm01u8TIP-CZT3DRhrvsku4HboeE3Oe2I8w4_SlmJf0c130_assertion
a
np:Assertion
.
dgn-np:NP407080.RAm01u8TIP-CZT3DRhrvsku4HboeE3Oe2I8w4_SlmJf0c130_provenance
a
np:Provenance
.
dgn-np:NP407080.RAm01u8TIP-CZT3DRhrvsku4HboeE3Oe2I8w4_SlmJf0c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP407080.RAm01u8TIP-CZT3DRhrvsku4HboeE3Oe2I8w4_SlmJf0c130_assertion
{
miriam-gene:345
a
ncit:C16612
.
lld:C0311277
a
ncit:C7057
.
dgn-gda:DGNb2d43f499ceb65a7c801e41909fd98c0
sio:SIO_000628
miriam-gene:345
,
lld:C0311277
;
a
sio:SIO_001121
.
}
dgn-np:NP407080.RAm01u8TIP-CZT3DRhrvsku4HboeE3Oe2I8w4_SlmJf0c130_provenance
{
dgn-np:NP407080.RAm01u8TIP-CZT3DRhrvsku4HboeE3Oe2I8w4_SlmJf0c130_assertion
dcterms:description
"[The odds ratios for MI for the APOC3*222 haplotype were 1.72 (95% CI: 1.16, 2.54) and 1.84 (1.31, 2.59) in subjects in the lowest quintiles of abdominal obesity and fasting hyperglycemia, respectively, and were 0.75 (0.54, 1.05) and 1.16 (0.85, 1.59) in subjects in the highest quintiles, respectively (P for interaction <0.05).]. 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:18541587
;
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:NP407080.RAm01u8TIP-CZT3DRhrvsku4HboeE3Oe2I8w4_SlmJf0c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:02+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" .
}