@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP66188.RAKRmqKHhxJN8NrxcyljTdTlRm65i7_pOZadHZHV6OPVc
> .
@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:NP66188.RAKRmqKHhxJN8NrxcyljTdTlRm65i7_pOZadHZHV6OPVc130_head
{
this:
np:hasAssertion
dgn-np:NP66188.RAKRmqKHhxJN8NrxcyljTdTlRm65i7_pOZadHZHV6OPVc130_assertion
;
np:hasProvenance
dgn-np:NP66188.RAKRmqKHhxJN8NrxcyljTdTlRm65i7_pOZadHZHV6OPVc130_provenance
;
np:hasPublicationInfo
dgn-np:NP66188.RAKRmqKHhxJN8NrxcyljTdTlRm65i7_pOZadHZHV6OPVc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP66188.RAKRmqKHhxJN8NrxcyljTdTlRm65i7_pOZadHZHV6OPVc130_assertion
a
np:Assertion
.
dgn-np:NP66188.RAKRmqKHhxJN8NrxcyljTdTlRm65i7_pOZadHZHV6OPVc130_provenance
a
np:Provenance
.
dgn-np:NP66188.RAKRmqKHhxJN8NrxcyljTdTlRm65i7_pOZadHZHV6OPVc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP66188.RAKRmqKHhxJN8NrxcyljTdTlRm65i7_pOZadHZHV6OPVc130_assertion
{
miriam-gene:5133
a
ncit:C16612
.
lld:C0018213
a
ncit:C7057
.
dgn-gda:DGN7fdebba4aeadf40ea9980fe9510c1d16
sio:SIO_000628
miriam-gene:5133
,
lld:C0018213
;
a
sio:SIO_001122
.
}
dgn-np:NP66188.RAKRmqKHhxJN8NrxcyljTdTlRm65i7_pOZadHZHV6OPVc130_provenance
{
dgn-np:NP66188.RAKRmqKHhxJN8NrxcyljTdTlRm65i7_pOZadHZHV6OPVc130_assertion
dcterms:description
"[This study has, for the first time, shown that small effects within PDCD1 may contribute towards the development of GD, supporting the hypothesis that much of the currently unknown genetic contribution to GD could be due to several small genetic effects with ORs 1.]. 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:17490403
;
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:NP66188.RAKRmqKHhxJN8NrxcyljTdTlRm65i7_pOZadHZHV6OPVc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:31+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" .
}