@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP718896.RAri2M3TX4CYOOPsbQv990E5hoGSJO81Ijrpr6I2q-4iI
> .
@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:NP718896.RAri2M3TX4CYOOPsbQv990E5hoGSJO81Ijrpr6I2q-4iI130_head
{
this:
np:hasAssertion
dgn-np:NP718896.RAri2M3TX4CYOOPsbQv990E5hoGSJO81Ijrpr6I2q-4iI130_assertion
;
np:hasProvenance
dgn-np:NP718896.RAri2M3TX4CYOOPsbQv990E5hoGSJO81Ijrpr6I2q-4iI130_provenance
;
np:hasPublicationInfo
dgn-np:NP718896.RAri2M3TX4CYOOPsbQv990E5hoGSJO81Ijrpr6I2q-4iI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP718896.RAri2M3TX4CYOOPsbQv990E5hoGSJO81Ijrpr6I2q-4iI130_assertion
a
np:Assertion
.
dgn-np:NP718896.RAri2M3TX4CYOOPsbQv990E5hoGSJO81Ijrpr6I2q-4iI130_provenance
a
np:Provenance
.
dgn-np:NP718896.RAri2M3TX4CYOOPsbQv990E5hoGSJO81Ijrpr6I2q-4iI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP718896.RAri2M3TX4CYOOPsbQv990E5hoGSJO81Ijrpr6I2q-4iI130_assertion
{
miriam-gene:2100
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN4badf9b8e7914a4675fde86141181f3b
sio:SIO_000628
miriam-gene:2100
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP718896.RAri2M3TX4CYOOPsbQv990E5hoGSJO81Ijrpr6I2q-4iI130_provenance
{
dgn-np:NP718896.RAri2M3TX4CYOOPsbQv990E5hoGSJO81Ijrpr6I2q-4iI130_assertion
dcterms:description
"[When the GG genotypes of the IL-6 and ERbeta SNPs were combined, the combination was much more robustly associated with PD, and especially with PD with an early age of onset, than respective GG genotype when analyzed separately.]. 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:15635591
;
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:NP718896.RAri2M3TX4CYOOPsbQv990E5hoGSJO81Ijrpr6I2q-4iI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:16+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" .
}