@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go
> .
@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:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_head
{
this:
np:hasAssertion
dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_assertion
;
np:hasProvenance
dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_provenance
;
np:hasPublicationInfo
dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_assertion
a
np:Assertion
.
dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_provenance
a
np:Provenance
.
dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_assertion
{
miriam-gene:3120
a
ncit:C16612
.
lld:C0277554
a
ncit:C7057
.
dgn-gda:DGN5cd20298b3322f07a3c1ee430757d7f3
sio:SIO_000628
miriam-gene:3120
,
lld:C0277554
;
a
sio:SIO_001121
.
}
dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_provenance
{
dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_assertion
dcterms:description
"[Although in the vast majority of patients with celiac disease, the HLA-DQ(alpha1*0501, beta1*0201) heterodimer encoded by the alleles HLA-DQA1*0501 and HLA-DQB1*0201 seems to confer the primary disease susceptibility, it cannot be excluded that other genes contribute to disease susceptibility, as indicated by the difference in concordance rates between monozygotic twins and HLA identical siblings (70% vs. 30%).]. 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:8820404
;
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:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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" .
}