@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP146043.RATtABso-pkrleAsyBk1q6BwrAmJt78W5ciau0onrsYsw
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
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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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
dgn-np:NP146043.RATtABso-pkrleAsyBk1q6BwrAmJt78W5ciau0onrsYsw130_provenance
;
np:hasPublicationInfo
dgn-np:NP146043.RATtABso-pkrleAsyBk1q6BwrAmJt78W5ciau0onrsYsw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP146043.RATtABso-pkrleAsyBk1q6BwrAmJt78W5ciau0onrsYsw130_assertion
a
np:Assertion
.
dgn-np:NP146043.RATtABso-pkrleAsyBk1q6BwrAmJt78W5ciau0onrsYsw130_provenance
a
np:Provenance
.
dgn-np:NP146043.RATtABso-pkrleAsyBk1q6BwrAmJt78W5ciau0onrsYsw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP146043.RATtABso-pkrleAsyBk1q6BwrAmJt78W5ciau0onrsYsw130_assertion
{
miriam-gene:26191
a
ncit:C16612
.
lld:C0040128
a
ncit:C7057
.
dgn-gda:DGN1c0b18f61b02cc9a4819260cb11ffa1d
sio:SIO_000628
miriam-gene:26191
,
lld:C0040128
;
a
sio:SIO_001122
.
}
dgn-np:NP146043.RATtABso-pkrleAsyBk1q6BwrAmJt78W5ciau0onrsYsw130_provenance
{
dgn-np:NP146043.RATtABso-pkrleAsyBk1q6BwrAmJt78W5ciau0onrsYsw130_assertion
dcterms:description
"[R620W polymorphism of PTPN22 is not major risk allele for SLE susceptibility in Caucasians from northern America, the UK, or Finland, but it appears to be risk factor for concurrent autoimmune diseases of autoimmune thyroid disease and SLE.]. 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:16052563
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP146043.RATtABso-pkrleAsyBk1q6BwrAmJt78W5ciau0onrsYsw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:16+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
<
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> , <
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" .
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pav:version
"v2.1.0" .
}