@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP525641.RAn2L0oZkL0Qray7meuwos8znLlEI_IFFhRKuQTyquSxw
> .
@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:NP525641.RAn2L0oZkL0Qray7meuwos8znLlEI_IFFhRKuQTyquSxw130_head
{
this:
np:hasAssertion
dgn-np:NP525641.RAn2L0oZkL0Qray7meuwos8znLlEI_IFFhRKuQTyquSxw130_assertion
;
np:hasProvenance
dgn-np:NP525641.RAn2L0oZkL0Qray7meuwos8znLlEI_IFFhRKuQTyquSxw130_provenance
;
np:hasPublicationInfo
dgn-np:NP525641.RAn2L0oZkL0Qray7meuwos8znLlEI_IFFhRKuQTyquSxw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP525641.RAn2L0oZkL0Qray7meuwos8znLlEI_IFFhRKuQTyquSxw130_assertion
a
np:Assertion
.
dgn-np:NP525641.RAn2L0oZkL0Qray7meuwos8znLlEI_IFFhRKuQTyquSxw130_provenance
a
np:Provenance
.
dgn-np:NP525641.RAn2L0oZkL0Qray7meuwos8znLlEI_IFFhRKuQTyquSxw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP525641.RAn2L0oZkL0Qray7meuwos8znLlEI_IFFhRKuQTyquSxw130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0002874
a
ncit:C7057
.
dgn-gda:DGN07ec9db252ebf410d190393c8d92d1af
sio:SIO_000628
miriam-gene:3126
,
lld:C0002874
;
a
sio:SIO_001121
.
}
dgn-np:NP525641.RAn2L0oZkL0Qray7meuwos8znLlEI_IFFhRKuQTyquSxw130_provenance
{
dgn-np:NP525641.RAn2L0oZkL0Qray7meuwos8znLlEI_IFFhRKuQTyquSxw130_assertion
dcterms:description
"[From the genetic viewpoint, it has been reported a significant increase frequency of the human leukocyte antigen HLA-DRB1(∗)15 in patients with AA as compared to ethnically matched healthy controls, this is true in different populations worldwide, which would suggests that this allele participates in the immune regulation of the disease.]. 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:22580214
;
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:NP525641.RAn2L0oZkL0Qray7meuwos8znLlEI_IFFhRKuQTyquSxw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:15+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" .
}