@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP576181.RAowbvObeF-pSRjM6p6IVLQk4dQeKQmht9FmMOgtTJ06E
> .
@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:NP576181.RAowbvObeF-pSRjM6p6IVLQk4dQeKQmht9FmMOgtTJ06E130_head
{
this:
np:hasAssertion
dgn-np:NP576181.RAowbvObeF-pSRjM6p6IVLQk4dQeKQmht9FmMOgtTJ06E130_assertion
;
np:hasProvenance
dgn-np:NP576181.RAowbvObeF-pSRjM6p6IVLQk4dQeKQmht9FmMOgtTJ06E130_provenance
;
np:hasPublicationInfo
dgn-np:NP576181.RAowbvObeF-pSRjM6p6IVLQk4dQeKQmht9FmMOgtTJ06E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP576181.RAowbvObeF-pSRjM6p6IVLQk4dQeKQmht9FmMOgtTJ06E130_assertion
a
np:Assertion
.
dgn-np:NP576181.RAowbvObeF-pSRjM6p6IVLQk4dQeKQmht9FmMOgtTJ06E130_provenance
a
np:Provenance
.
dgn-np:NP576181.RAowbvObeF-pSRjM6p6IVLQk4dQeKQmht9FmMOgtTJ06E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP576181.RAowbvObeF-pSRjM6p6IVLQk4dQeKQmht9FmMOgtTJ06E130_assertion
{
miriam-gene:26191
a
ncit:C16612
.
lld:C0553662
a
ncit:C7057
.
dgn-gda:DGN54550b423cc8a857ad0e4969edf5056f
sio:SIO_000628
miriam-gene:26191
,
lld:C0553662
;
a
sio:SIO_001121
.
}
dgn-np:NP576181.RAowbvObeF-pSRjM6p6IVLQk4dQeKQmht9FmMOgtTJ06E130_provenance
{
dgn-np:NP576181.RAowbvObeF-pSRjM6p6IVLQk4dQeKQmht9FmMOgtTJ06E130_assertion
dcterms:description
"[The discovery that a single-nucleotide polymorphism (SNP) in lymphoid tyrosine phosphatase (LYP), encoded by the PTPN22 gene, is associated with type 1 diabetes (T1D) has now been verified by numerous studies and has been expanded to rheumatoid arthritis, juvenile rheumatoid arthritis (JRA), systemic lupus erythematosus, Graves' disease, generalized vitiligo and other human autoimmune diseases.]. 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:17729039
;
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:NP576181.RAowbvObeF-pSRjM6p6IVLQk4dQeKQmht9FmMOgtTJ06E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:47+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" .
}