@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP408318.RA0oGNbcuR-P1dWGpLwaAql2Kkt3EVRqr85gQKzFhjqlE
> .
@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:NP408318.RA0oGNbcuR-P1dWGpLwaAql2Kkt3EVRqr85gQKzFhjqlE130_head
{
this:
np:hasAssertion
dgn-np:NP408318.RA0oGNbcuR-P1dWGpLwaAql2Kkt3EVRqr85gQKzFhjqlE130_assertion
;
np:hasProvenance
dgn-np:NP408318.RA0oGNbcuR-P1dWGpLwaAql2Kkt3EVRqr85gQKzFhjqlE130_provenance
;
np:hasPublicationInfo
dgn-np:NP408318.RA0oGNbcuR-P1dWGpLwaAql2Kkt3EVRqr85gQKzFhjqlE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP408318.RA0oGNbcuR-P1dWGpLwaAql2Kkt3EVRqr85gQKzFhjqlE130_assertion
a
np:Assertion
.
dgn-np:NP408318.RA0oGNbcuR-P1dWGpLwaAql2Kkt3EVRqr85gQKzFhjqlE130_provenance
a
np:Provenance
.
dgn-np:NP408318.RA0oGNbcuR-P1dWGpLwaAql2Kkt3EVRqr85gQKzFhjqlE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP408318.RA0oGNbcuR-P1dWGpLwaAql2Kkt3EVRqr85gQKzFhjqlE130_assertion
{
miriam-gene:26191
a
ncit:C16612
.
lld:C0015397
a
ncit:C7057
.
dgn-gda:DGN50e4fd1abe36310ffbc08c71a9b7baa6
sio:SIO_000628
miriam-gene:26191
,
lld:C0015397
;
a
sio:SIO_001121
.
}
dgn-np:NP408318.RA0oGNbcuR-P1dWGpLwaAql2Kkt3EVRqr85gQKzFhjqlE130_provenance
{
dgn-np:NP408318.RA0oGNbcuR-P1dWGpLwaAql2Kkt3EVRqr85gQKzFhjqlE130_assertion
dcterms:description
"[The distribution of PTPN22 alleles and genotypes among patients and controls was compared, and correlation was sought between PTPN22 'T' and sex, tobacco smoking status, family history of GD, age of disease onset, presence (and severity) of ophthalmopathy, and presence of the CTLA4 A49G or DRB1*03 alleles.]. 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:15943829
;
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:NP408318.RA0oGNbcuR-P1dWGpLwaAql2Kkt3EVRqr85gQKzFhjqlE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:03+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" .
}