@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP497210.RAMWXXvUWES4Wx9KrQ-cK6XsB8k28AuWiNkqEgv0Mim0g
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP497210.RAMWXXvUWES4Wx9KrQ-cK6XsB8k28AuWiNkqEgv0Mim0g130_assertion
;
np:hasProvenance
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;
a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP497210.RAMWXXvUWES4Wx9KrQ-cK6XsB8k28AuWiNkqEgv0Mim0g130_provenance
a
np:Provenance
.
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a
np:PublicationInfo
.
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{
miriam-gene:7267
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGN8faab2ee47bdfb3f5060431b82726b1b
sio:SIO_000628
miriam-gene:7267
,
lld:C0011854
;
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.
}
dgn-np:NP497210.RAMWXXvUWES4Wx9KrQ-cK6XsB8k28AuWiNkqEgv0Mim0g130_provenance
{
dgn-np:NP497210.RAMWXXvUWES4Wx9KrQ-cK6XsB8k28AuWiNkqEgv0Mim0g130_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:NP497210.RAMWXXvUWES4Wx9KrQ-cK6XsB8k28AuWiNkqEgv0Mim0g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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
<
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> , <
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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pav:version
"v2.1.0" .
}