@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP476757.RAdUHGVAxj3cmP5yTGNz0ZB2gA09J6kYgLiPqaC5OmnvY
> .
@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:NP476757.RAdUHGVAxj3cmP5yTGNz0ZB2gA09J6kYgLiPqaC5OmnvY130_head
{
this:
np:hasAssertion
dgn-np:NP476757.RAdUHGVAxj3cmP5yTGNz0ZB2gA09J6kYgLiPqaC5OmnvY130_assertion
;
np:hasProvenance
dgn-np:NP476757.RAdUHGVAxj3cmP5yTGNz0ZB2gA09J6kYgLiPqaC5OmnvY130_provenance
;
np:hasPublicationInfo
dgn-np:NP476757.RAdUHGVAxj3cmP5yTGNz0ZB2gA09J6kYgLiPqaC5OmnvY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP476757.RAdUHGVAxj3cmP5yTGNz0ZB2gA09J6kYgLiPqaC5OmnvY130_assertion
a
np:Assertion
.
dgn-np:NP476757.RAdUHGVAxj3cmP5yTGNz0ZB2gA09J6kYgLiPqaC5OmnvY130_provenance
a
np:Provenance
.
dgn-np:NP476757.RAdUHGVAxj3cmP5yTGNz0ZB2gA09J6kYgLiPqaC5OmnvY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP476757.RAdUHGVAxj3cmP5yTGNz0ZB2gA09J6kYgLiPqaC5OmnvY130_assertion
{
miriam-gene:3303
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN62656fd8846a8bc2c7c02f01c02428d0
sio:SIO_000628
miriam-gene:3303
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP476757.RAdUHGVAxj3cmP5yTGNz0ZB2gA09J6kYgLiPqaC5OmnvY130_provenance
{
dgn-np:NP476757.RAdUHGVAxj3cmP5yTGNz0ZB2gA09J6kYgLiPqaC5OmnvY130_assertion
dcterms:description
"[Our data indicate that HSP70-2 gene polymorphism as opposed to the other ethnic groups does not appear to be relevant in SLE susceptibility in Mexican patients and that the distribution of the different alleles depend on the frequency of HLA alleles associated with them.]. 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:11196683
;
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:NP476757.RAdUHGVAxj3cmP5yTGNz0ZB2gA09J6kYgLiPqaC5OmnvY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}