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http://rdf.disgenet.org/nanopublications.trig#NP766991.RAA9PyEp4rboR5MNrTi-pL_iZ7can63SMX4V96pyInuls
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP766991.RAA9PyEp4rboR5MNrTi-pL_iZ7can63SMX4V96pyInuls130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP766991.RAA9PyEp4rboR5MNrTi-pL_iZ7can63SMX4V96pyInuls130_provenance
a
np:Provenance
.
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a
np:PublicationInfo
.
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dgn-np:NP766991.RAA9PyEp4rboR5MNrTi-pL_iZ7can63SMX4V96pyInuls130_assertion
{
miriam-gene:1861
a
ncit:C16612
.
lld:C0001403
a
ncit:C7057
.
dgn-gda:DGN393f366324a126ae5242a22ef1fed0f4
sio:SIO_000628
miriam-gene:1861
,
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;
a
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.
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dgn-np:NP766991.RAA9PyEp4rboR5MNrTi-pL_iZ7can63SMX4V96pyInuls130_provenance
{
dgn-np:NP766991.RAA9PyEp4rboR5MNrTi-pL_iZ7can63SMX4V96pyInuls130_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
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sio:SIO_000772
miriam-pubmed:12392510
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
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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 .
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dgn-np:NP766991.RAA9PyEp4rboR5MNrTi-pL_iZ7can63SMX4V96pyInuls130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
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prv:usedData
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pav:authoredBy
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> , <
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> , <
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> ;
pav:createdBy
<
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pav:version
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