@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP752359.RAQgmLe52K8puvS-r-NRMu0fRdDn36f37L4p6jw22mqms
> .
@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:NP752359.RAQgmLe52K8puvS-r-NRMu0fRdDn36f37L4p6jw22mqms130_head
{
this:
np:hasAssertion
dgn-np:NP752359.RAQgmLe52K8puvS-r-NRMu0fRdDn36f37L4p6jw22mqms130_assertion
;
np:hasProvenance
dgn-np:NP752359.RAQgmLe52K8puvS-r-NRMu0fRdDn36f37L4p6jw22mqms130_provenance
;
np:hasPublicationInfo
dgn-np:NP752359.RAQgmLe52K8puvS-r-NRMu0fRdDn36f37L4p6jw22mqms130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP752359.RAQgmLe52K8puvS-r-NRMu0fRdDn36f37L4p6jw22mqms130_assertion
a
np:Assertion
.
dgn-np:NP752359.RAQgmLe52K8puvS-r-NRMu0fRdDn36f37L4p6jw22mqms130_provenance
a
np:Provenance
.
dgn-np:NP752359.RAQgmLe52K8puvS-r-NRMu0fRdDn36f37L4p6jw22mqms130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP752359.RAQgmLe52K8puvS-r-NRMu0fRdDn36f37L4p6jw22mqms130_assertion
{
miriam-gene:3052
a
ncit:C16612
.
lld:C0178468
a
ncit:C7057
.
dgn-gda:DGNc181fe9257afe33f29970cc61fbba684
sio:SIO_000628
miriam-gene:3052
,
lld:C0178468
;
a
sio:SIO_001121
.
}
dgn-np:NP752359.RAQgmLe52K8puvS-r-NRMu0fRdDn36f37L4p6jw22mqms130_provenance
{
dgn-np:NP752359.RAQgmLe52K8puvS-r-NRMu0fRdDn36f37L4p6jw22mqms130_assertion
dcterms:description
"[The CTLA-4 gene showed evidence for linkage only when individuals with both T1D and AITD were considered affected (MLS, 1.7), and the insulin VNTR showed evidence for linkage when individuals with either T1D or AITD were considered affected (MLS, 1.9); i.e.]. 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:15928253
;
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:NP752359.RAQgmLe52K8puvS-r-NRMu0fRdDn36f37L4p6jw22mqms130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}