@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp_Ja0DTTDxNhtquPtAM
> .
@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:NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp_Ja0DTTDxNhtquPtAM130_head
{
this:
np:hasAssertion
dgn-np:NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp_Ja0DTTDxNhtquPtAM130_assertion
;
np:hasProvenance
dgn-np:NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp_Ja0DTTDxNhtquPtAM130_provenance
;
np:hasPublicationInfo
dgn-np:NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp_Ja0DTTDxNhtquPtAM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp_Ja0DTTDxNhtquPtAM130_assertion
a
np:Assertion
.
dgn-np:NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp_Ja0DTTDxNhtquPtAM130_provenance
a
np:Provenance
.
dgn-np:NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp_Ja0DTTDxNhtquPtAM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp_Ja0DTTDxNhtquPtAM130_assertion
{
miriam-gene:5346
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGNe4a8b575b3f69d2b4ce522a26627ae79
sio:SIO_000628
miriam-gene:5346
,
lld:C0524620
;
a
sio:SIO_001122
.
}
dgn-np:NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp_Ja0DTTDxNhtquPtAM130_provenance
{
dgn-np:NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp_Ja0DTTDxNhtquPtAM130_assertion
dcterms:description
"[The minor A allele at PLIN4 was associated with higher risk of MS at baseline, whereas the PLIN6 SNP was associated with better weight loss, suggesting that these polymorphisms may predict outcome strategies based on multidisciplinary treatment for OCA.]. 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:18812483
;
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:NP68205.RAUgcVzeZB8ILDX6lsxb5fWH5mp_Ja0DTTDxNhtquPtAM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:32+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" .
}