@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP518378.RAqmLFd_eKA3VJB8a6lg5nNTiOkhR-XM1-v5vE11xTbBw
> .
@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:NP518378.RAqmLFd_eKA3VJB8a6lg5nNTiOkhR-XM1-v5vE11xTbBw130_head
{
this:
np:hasAssertion
dgn-np:NP518378.RAqmLFd_eKA3VJB8a6lg5nNTiOkhR-XM1-v5vE11xTbBw130_assertion
;
np:hasProvenance
dgn-np:NP518378.RAqmLFd_eKA3VJB8a6lg5nNTiOkhR-XM1-v5vE11xTbBw130_provenance
;
np:hasPublicationInfo
dgn-np:NP518378.RAqmLFd_eKA3VJB8a6lg5nNTiOkhR-XM1-v5vE11xTbBw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP518378.RAqmLFd_eKA3VJB8a6lg5nNTiOkhR-XM1-v5vE11xTbBw130_assertion
a
np:Assertion
.
dgn-np:NP518378.RAqmLFd_eKA3VJB8a6lg5nNTiOkhR-XM1-v5vE11xTbBw130_provenance
a
np:Provenance
.
dgn-np:NP518378.RAqmLFd_eKA3VJB8a6lg5nNTiOkhR-XM1-v5vE11xTbBw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP518378.RAqmLFd_eKA3VJB8a6lg5nNTiOkhR-XM1-v5vE11xTbBw130_assertion
{
miriam-gene:9388
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNa4dc14c382b0d4f4f393c22e39773c22
sio:SIO_000628
miriam-gene:9388
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP518378.RAqmLFd_eKA3VJB8a6lg5nNTiOkhR-XM1-v5vE11xTbBw130_provenance
{
dgn-np:NP518378.RAqmLFd_eKA3VJB8a6lg5nNTiOkhR-XM1-v5vE11xTbBw130_assertion
dcterms:description
"[Small studies in selected populations have reported higher HDL-C levels among carriers of the common T111I variant in LIPG, but whether this variant is associated with plasma lipids and risk of coronary heart disease (CHD) in the general population is unclear.]. 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:19411665
;
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:NP518378.RAqmLFd_eKA3VJB8a6lg5nNTiOkhR-XM1-v5vE11xTbBw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:08+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" .
}