@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8
> .
@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:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_head
{
this:
np:hasAssertion
dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_assertion
;
np:hasProvenance
dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_provenance
;
np:hasPublicationInfo
dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_assertion
a
np:Assertion
.
dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_provenance
a
np:Provenance
.
dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_assertion
{
miriam-gene:26191
a
ncit:C16612
.
lld:C0015397
a
ncit:C7057
.
dgn-gda:DGN8434f29d0a9122306de435cb42a03fce
sio:SIO_000628
miriam-gene:26191
,
lld:C0015397
;
a
sio:SIO_001121
.
}
dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_provenance
{
dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_assertion
dcterms:description
"[No other statistically significant associations between the ESR2 genotype and GD subsets were found (age of onset, smoking, clinically evident ophthalmopathy, family history of GD, and PTPN22 and CTLA4 (CT60) genotypes were analysed).]. 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:17941906
;
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:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:33+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" .
}