@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP76526.RAopaAVorlCe8ELfLFoNoeP0vBeGc5kpSLO9oUdEMxXI4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP76526.RAopaAVorlCe8ELfLFoNoeP0vBeGc5kpSLO9oUdEMxXI4130_head
{
this:
np:hasAssertion
dgn-np:NP76526.RAopaAVorlCe8ELfLFoNoeP0vBeGc5kpSLO9oUdEMxXI4130_assertion
;
np:hasProvenance
dgn-np:NP76526.RAopaAVorlCe8ELfLFoNoeP0vBeGc5kpSLO9oUdEMxXI4130_provenance
;
np:hasPublicationInfo
dgn-np:NP76526.RAopaAVorlCe8ELfLFoNoeP0vBeGc5kpSLO9oUdEMxXI4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP76526.RAopaAVorlCe8ELfLFoNoeP0vBeGc5kpSLO9oUdEMxXI4130_assertion
a
np:Assertion
.
dgn-np:NP76526.RAopaAVorlCe8ELfLFoNoeP0vBeGc5kpSLO9oUdEMxXI4130_provenance
a
np:Provenance
.
dgn-np:NP76526.RAopaAVorlCe8ELfLFoNoeP0vBeGc5kpSLO9oUdEMxXI4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP76526.RAopaAVorlCe8ELfLFoNoeP0vBeGc5kpSLO9oUdEMxXI4130_assertion
{
miriam-gene:345
a
ncit:C16612
.
lld:C1522137
a
ncit:C7057
.
dgn-gda:DGNf8b025e5f05917ab91e79418fbd96a97
sio:SIO_000628
miriam-gene:345
,
lld:C1522137
;
a
sio:SIO_001122
.
}
dgn-np:NP76526.RAopaAVorlCe8ELfLFoNoeP0vBeGc5kpSLO9oUdEMxXI4130_provenance
{
dgn-np:NP76526.RAopaAVorlCe8ELfLFoNoeP0vBeGc5kpSLO9oUdEMxXI4130_assertion
dcterms:description
"[The minor allele S2, which was associated with both CHD with HTG and NIDDM with HTG and may contribute to the susceptibility of hypertriglyceridemia in CHD and NIDDM patients, may be one of the genetic predispositions to both CHD with HTG and NIDDM with H]. 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:15715433
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP76526.RAopaAVorlCe8ELfLFoNoeP0vBeGc5kpSLO9oUdEMxXI4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:22+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}