@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP376738.RAxunSZOckO2ukZz0UcVXSR_6omq4KUF5quYK7Qt4s4JE
> .
@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:NP376738.RAxunSZOckO2ukZz0UcVXSR_6omq4KUF5quYK7Qt4s4JE130_head
{
this:
np:hasAssertion
dgn-np:NP376738.RAxunSZOckO2ukZz0UcVXSR_6omq4KUF5quYK7Qt4s4JE130_assertion
;
np:hasProvenance
dgn-np:NP376738.RAxunSZOckO2ukZz0UcVXSR_6omq4KUF5quYK7Qt4s4JE130_provenance
;
np:hasPublicationInfo
dgn-np:NP376738.RAxunSZOckO2ukZz0UcVXSR_6omq4KUF5quYK7Qt4s4JE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP376738.RAxunSZOckO2ukZz0UcVXSR_6omq4KUF5quYK7Qt4s4JE130_assertion
a
np:Assertion
.
dgn-np:NP376738.RAxunSZOckO2ukZz0UcVXSR_6omq4KUF5quYK7Qt4s4JE130_provenance
a
np:Provenance
.
dgn-np:NP376738.RAxunSZOckO2ukZz0UcVXSR_6omq4KUF5quYK7Qt4s4JE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP376738.RAxunSZOckO2ukZz0UcVXSR_6omq4KUF5quYK7Qt4s4JE130_assertion
{
miriam-gene:4023
a
ncit:C16612
.
lld:C0242339
a
ncit:C7057
.
dgn-gda:DGN2dcc8326205a0e11fb94d014ab572d0d
sio:SIO_000628
miriam-gene:4023
,
lld:C0242339
;
a
sio:SIO_001121
.
}
dgn-np:NP376738.RAxunSZOckO2ukZz0UcVXSR_6omq4KUF5quYK7Qt4s4JE130_provenance
{
dgn-np:NP376738.RAxunSZOckO2ukZz0UcVXSR_6omq4KUF5quYK7Qt4s4JE130_assertion
dcterms:description
"[Our data suggest that the polymorphisms at the LPL gene, as the linkage markers with an aetiologic mutation at or around LPL gene, may constitute one of the genetic determinants for the population variation in plasma TG levels, as well as for the common dyslipidemia in Chinese populations.]. 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:9387400
;
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:NP376738.RAxunSZOckO2ukZz0UcVXSR_6omq4KUF5quYK7Qt4s4JE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:40+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" .
}