@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP451636.RAGrf5LMKJxMLBJ4d0KzVd9tYc1X_N6yds7KXSIQGyw7k
> .
@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:NP451636.RAGrf5LMKJxMLBJ4d0KzVd9tYc1X_N6yds7KXSIQGyw7k130_head
{
this:
np:hasAssertion
dgn-np:NP451636.RAGrf5LMKJxMLBJ4d0KzVd9tYc1X_N6yds7KXSIQGyw7k130_assertion
;
np:hasProvenance
dgn-np:NP451636.RAGrf5LMKJxMLBJ4d0KzVd9tYc1X_N6yds7KXSIQGyw7k130_provenance
;
np:hasPublicationInfo
dgn-np:NP451636.RAGrf5LMKJxMLBJ4d0KzVd9tYc1X_N6yds7KXSIQGyw7k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP451636.RAGrf5LMKJxMLBJ4d0KzVd9tYc1X_N6yds7KXSIQGyw7k130_assertion
a
np:Assertion
.
dgn-np:NP451636.RAGrf5LMKJxMLBJ4d0KzVd9tYc1X_N6yds7KXSIQGyw7k130_provenance
a
np:Provenance
.
dgn-np:NP451636.RAGrf5LMKJxMLBJ4d0KzVd9tYc1X_N6yds7KXSIQGyw7k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP451636.RAGrf5LMKJxMLBJ4d0KzVd9tYc1X_N6yds7KXSIQGyw7k130_assertion
{
miriam-gene:3753
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGN9087b671f392b8d3234876c8b08cf203
sio:SIO_000628
miriam-gene:3753
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP451636.RAGrf5LMKJxMLBJ4d0KzVd9tYc1X_N6yds7KXSIQGyw7k130_provenance
{
dgn-np:NP451636.RAGrf5LMKJxMLBJ4d0KzVd9tYc1X_N6yds7KXSIQGyw7k130_assertion
dcterms:description
"[However, none of the SNPs showed association to T1D in the complete material, whereas some evidence for association to T1D of variants of the TTC3, OLIG2, KCNE1, and CBR1 genes was observed in conditioned analyses.]. 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:15635070
;
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:NP451636.RAGrf5LMKJxMLBJ4d0KzVd9tYc1X_N6yds7KXSIQGyw7k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:29+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" .
}