@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP58106.RACWiewnSyT4BTwfoqy3Rtrw1aeAsQv2_8sBlnJY2hITs
> .
@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:NP58106.RACWiewnSyT4BTwfoqy3Rtrw1aeAsQv2_8sBlnJY2hITs130_head
{
this:
np:hasAssertion
dgn-np:NP58106.RACWiewnSyT4BTwfoqy3Rtrw1aeAsQv2_8sBlnJY2hITs130_assertion
;
np:hasProvenance
dgn-np:NP58106.RACWiewnSyT4BTwfoqy3Rtrw1aeAsQv2_8sBlnJY2hITs130_provenance
;
np:hasPublicationInfo
dgn-np:NP58106.RACWiewnSyT4BTwfoqy3Rtrw1aeAsQv2_8sBlnJY2hITs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP58106.RACWiewnSyT4BTwfoqy3Rtrw1aeAsQv2_8sBlnJY2hITs130_assertion
a
np:Assertion
.
dgn-np:NP58106.RACWiewnSyT4BTwfoqy3Rtrw1aeAsQv2_8sBlnJY2hITs130_provenance
a
np:Provenance
.
dgn-np:NP58106.RACWiewnSyT4BTwfoqy3Rtrw1aeAsQv2_8sBlnJY2hITs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP58106.RACWiewnSyT4BTwfoqy3Rtrw1aeAsQv2_8sBlnJY2hITs130_assertion
{
miriam-gene:3117
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNad3e6f6b397e935df3c1e11e938d6402
sio:SIO_000628
miriam-gene:3117
,
lld:C0024141
;
a
sio:SIO_001122
.
}
dgn-np:NP58106.RACWiewnSyT4BTwfoqy3Rtrw1aeAsQv2_8sBlnJY2hITs130_provenance
{
dgn-np:NP58106.RACWiewnSyT4BTwfoqy3Rtrw1aeAsQv2_8sBlnJY2hITs130_assertion
dcterms:description
"[The results suggest that the DRB1*0301 is the principal class II allele associated with the genetic susceptibility to SLE in Mexican patients and that the presence of a specific haplotype of the homologous chromosome in patients with DRB1*0407-DQA1*03-DQB1*0302 and DRB1*1501-DQA1*0102-DQB1*0602 haplotypes could have an additive effect on the susceptibility to the disease. Finally, the low frequency of the DRB1*0301 and DRB1*1501 alleles in the control population suggests that the genetic admixture between Mexican Indians and Caucasian populations was an event that could have increased the risk of Mexicans to develop SLE.]. 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:11476905
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP58106.RACWiewnSyT4BTwfoqy3Rtrw1aeAsQv2_8sBlnJY2hITs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}