@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0
> .
@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:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_head
{
this:
np:hasAssertion
dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_assertion
;
np:hasProvenance
dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_provenance
;
np:hasPublicationInfo
dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_assertion
a
np:Assertion
.
dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_provenance
a
np:Provenance
.
dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_assertion
{
miriam-gene:1493
a
ncit:C16612
.
lld:C0339143
a
ncit:C7057
.
dgn-gda:DGN2f9672fff50b8444d7d194b4491a3cfe
sio:SIO_000628
miriam-gene:1493
,
lld:C0339143
;
a
sio:SIO_001121
.
}
dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_provenance
{
dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_assertion
dcterms:description
"[We analyzed the A(49)G exon 1 CTLA-4 gene polymorphism in 99 unrelated Polish patients with GD, of whom 50 had clinically evident GO (NOSPECS class III and higher), and 154 matched healthy subjects from the Lower Silesia region.]. 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:15507878
;
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:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:11+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" .
}