@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP479499.RACVTY1-M0prFXiif-775pgakTtyo5_duuUgMX8Gi2aEQ
> .
@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:NP479499.RACVTY1-M0prFXiif-775pgakTtyo5_duuUgMX8Gi2aEQ130_head
{
this:
np:hasAssertion
dgn-np:NP479499.RACVTY1-M0prFXiif-775pgakTtyo5_duuUgMX8Gi2aEQ130_assertion
;
np:hasProvenance
dgn-np:NP479499.RACVTY1-M0prFXiif-775pgakTtyo5_duuUgMX8Gi2aEQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP479499.RACVTY1-M0prFXiif-775pgakTtyo5_duuUgMX8Gi2aEQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP479499.RACVTY1-M0prFXiif-775pgakTtyo5_duuUgMX8Gi2aEQ130_assertion
a
np:Assertion
.
dgn-np:NP479499.RACVTY1-M0prFXiif-775pgakTtyo5_duuUgMX8Gi2aEQ130_provenance
a
np:Provenance
.
dgn-np:NP479499.RACVTY1-M0prFXiif-775pgakTtyo5_duuUgMX8Gi2aEQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP479499.RACVTY1-M0prFXiif-775pgakTtyo5_duuUgMX8Gi2aEQ130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0266273
a
ncit:C7057
.
dgn-gda:DGN78fca626ae94865f2d6e68206d138344
sio:SIO_000628
miriam-gene:3126
,
lld:C0266273
;
a
sio:SIO_001121
.
}
dgn-np:NP479499.RACVTY1-M0prFXiif-775pgakTtyo5_duuUgMX8Gi2aEQ130_provenance
{
dgn-np:NP479499.RACVTY1-M0prFXiif-775pgakTtyo5_duuUgMX8Gi2aEQ130_assertion
dcterms:description
"[In the current study, we ascertained the haplotypes of 57 Caucasian patients with Addison's disease composed of these genetic markers and compared them either with 72 general population controls or with 105 child controls carrying Addison's disease high-risk DR3-DQ2/DR4-DQ8 genotypes.]. 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:12392510
;
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:NP479499.RACVTY1-M0prFXiif-775pgakTtyo5_duuUgMX8Gi2aEQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:47+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" .
}