@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U
> .
@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:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_head
{
this:
np:hasAssertion
dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_assertion
;
np:hasProvenance
dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_provenance
;
np:hasPublicationInfo
dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_assertion
a
np:Assertion
.
dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_provenance
a
np:Provenance
.
dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_assertion
{
miriam-gene:5360
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN59eecdaacb9663dca84f35ffd1dfe08c
sio:SIO_000628
miriam-gene:5360
,
lld:C0028754
;
a
sio:SIO_001122
.
}
dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_provenance
{
dgn-np:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_assertion
dcterms:description
"[ Intronic variants of the PLTP gene are significantly associated with obesity-related phenotypes. Considering the number and the relevance of candidate genes surrounding the PLTP locus and the absence of missense polymorphisms in the coding region, the associations could be mediated by a second gene allele in linkage disequilibrium with the marker locus.]. 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:15953936
;
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:NP53067.RAiV7FEmviWnVBjzvm03crLzLAq8pHWnu7EPRb2lvby6U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}