@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48454.RA7iWIfmeZrYFq7NfzoWM_AiPRXjcCBuLjV7yg5bOekDo
> .
@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:NP48454.RA7iWIfmeZrYFq7NfzoWM_AiPRXjcCBuLjV7yg5bOekDo130_head
{
this:
np:hasAssertion
dgn-np:NP48454.RA7iWIfmeZrYFq7NfzoWM_AiPRXjcCBuLjV7yg5bOekDo130_assertion
;
np:hasProvenance
dgn-np:NP48454.RA7iWIfmeZrYFq7NfzoWM_AiPRXjcCBuLjV7yg5bOekDo130_provenance
;
np:hasPublicationInfo
dgn-np:NP48454.RA7iWIfmeZrYFq7NfzoWM_AiPRXjcCBuLjV7yg5bOekDo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48454.RA7iWIfmeZrYFq7NfzoWM_AiPRXjcCBuLjV7yg5bOekDo130_assertion
a
np:Assertion
.
dgn-np:NP48454.RA7iWIfmeZrYFq7NfzoWM_AiPRXjcCBuLjV7yg5bOekDo130_provenance
a
np:Provenance
.
dgn-np:NP48454.RA7iWIfmeZrYFq7NfzoWM_AiPRXjcCBuLjV7yg5bOekDo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48454.RA7iWIfmeZrYFq7NfzoWM_AiPRXjcCBuLjV7yg5bOekDo130_assertion
{
miriam-gene:337
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGNd6d69ed76f9578bc01fb410589c22a06
sio:SIO_000628
miriam-gene:337
,
lld:C0027051
;
a
sio:SIO_001122
.
}
dgn-np:NP48454.RA7iWIfmeZrYFq7NfzoWM_AiPRXjcCBuLjV7yg5bOekDo130_provenance
{
dgn-np:NP48454.RA7iWIfmeZrYFq7NfzoWM_AiPRXjcCBuLjV7yg5bOekDo130_assertion
dcterms:description
"[ In this prospective study of apparently healthy middle-aged US men, carriers of the X1-S2 haplotype in the APOA1 XmnI and APOC3 SstI variants across the APOA1/C3/A4 gene cluster had higher TG levels, but there was no evidence for significant associations between these two common variants or haplotypes defined by them and risk of incident MI in this cohort.]. 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:15488874
;
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:NP48454.RA7iWIfmeZrYFq7NfzoWM_AiPRXjcCBuLjV7yg5bOekDo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}