@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_assertion
;
np:hasProvenance
dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_provenance
;
np:hasPublicationInfo
dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_assertion
a
np:Assertion
.
dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_provenance
a
np:Provenance
.
dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_assertion
{
miriam-gene:26191
a
ncit:C16612
.
lld:C0036421
a
ncit:C7057
.
dgn-gda:DGN86d81e5ce19cd458ca7025a402958232
sio:SIO_000628
miriam-gene:26191
,
lld:C0036421
;
a
sio:SIO_001121
.
}
dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_provenance
{
dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_assertion
dcterms:description
"[The association of subsets of SSc with the PTPN22 R620W polymorphism further strengthens the classification of SSc within the spectrum of autoimmune diseases and strongly suggests the involvement of common susceptibility genes and similarly disordered immunoregulatory pathways.]. 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:17133608
;
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:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:36+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" .
}