@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP162000.RAd2jsIb05RfO9yQe2MrFYUJRGjGBV5mUoA_Jl9O8HyVc
> .
@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:NP162000.RAd2jsIb05RfO9yQe2MrFYUJRGjGBV5mUoA_Jl9O8HyVc130_head
{
this:
np:hasAssertion
dgn-np:NP162000.RAd2jsIb05RfO9yQe2MrFYUJRGjGBV5mUoA_Jl9O8HyVc130_assertion
;
np:hasProvenance
dgn-np:NP162000.RAd2jsIb05RfO9yQe2MrFYUJRGjGBV5mUoA_Jl9O8HyVc130_provenance
;
np:hasPublicationInfo
dgn-np:NP162000.RAd2jsIb05RfO9yQe2MrFYUJRGjGBV5mUoA_Jl9O8HyVc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP162000.RAd2jsIb05RfO9yQe2MrFYUJRGjGBV5mUoA_Jl9O8HyVc130_assertion
a
np:Assertion
.
dgn-np:NP162000.RAd2jsIb05RfO9yQe2MrFYUJRGjGBV5mUoA_Jl9O8HyVc130_provenance
a
np:Provenance
.
dgn-np:NP162000.RAd2jsIb05RfO9yQe2MrFYUJRGjGBV5mUoA_Jl9O8HyVc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP162000.RAd2jsIb05RfO9yQe2MrFYUJRGjGBV5mUoA_Jl9O8HyVc130_assertion
{
miriam-gene:52
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGN1d883e7ab0d6cb025200b70d9cb0fa14
sio:SIO_000628
miriam-gene:52
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP162000.RAd2jsIb05RfO9yQe2MrFYUJRGjGBV5mUoA_Jl9O8HyVc130_provenance
{
dgn-np:NP162000.RAd2jsIb05RfO9yQe2MrFYUJRGjGBV5mUoA_Jl9O8HyVc130_assertion
dcterms:description
"[A functional single nucleotide polymorphism (SNP) of PTPN22 gene encoding the protein tyrosine phosphatase has been reported to be associated with autoimmune disorders such as rheumatoid arthritis, systemic lupus erythematosus and type I diabetes.]. 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:17868256
;
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:NP162000.RAd2jsIb05RfO9yQe2MrFYUJRGjGBV5mUoA_Jl9O8HyVc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}